Article Text

Original research
Prospective evaluation to characterize the real-world performance of the EMBOVAC aspiration catheter for neurothrombectomy: a post-market clinical follow-up trial
  1. Mariangela Piano1,
  2. Olav Jansen2,
  3. Gaultier Marnat3,
  4. Benjamin Gory4,
  5. Hannes Nordmeyer5,6,
  6. Bernd Eckert7,
  7. Alessandro Pedicelli8,
  8. Christophe Cognard9,
  9. Christian Loehr10,
  10. Matteo Zanoni11,
  11. Axel Schaefer12,
  12. Antonio Macera13,
  13. Jens Fiehler14,15,
  14. Karen Doyle16,
  15. Kyriakos Lobotesis17
  1. 1Neuroradiology, Ospedale Niguarda Ca' Granda, Milano, Italy
  2. 2University Hospital, Christian-Albrechts – University Kiel, Kiel, Germany
  3. 3Interventional and Diagnostic Neuroradiology, Bordeaux University Hospital, Bordeaux, France
  4. 4Department of Diagnostic and Interventional Neuroradiology, CHRU Nancy, Nancy, Lorraine, France
  5. 5Neuroradiology, Städtisches Klinikum Solingen, Department of Diagnostic and Interventional Neuroradiology, Solingen, Germany
  6. 6Witten/Herdecke University, Department of Health, School of Medicine, Witten, Germany
  7. 7Neuroradiology, Asklepios Clinic Altona, Hamburg, Germany
  8. 8Radiological Sciences, Catholic University of Sacred Heart, “A. Gemelli” Hospital, Rome, Italy
  9. 9Diagnostic and Therapeutic Neuroradiology, Hôpital Purpan, Toulouse, France
  10. 10Department of Radiology and Neuroradiology, Klinikum Vest GmbH, Recklinghausen, Nordrhein-Westfalen, Germany
  11. 11Department of Medicine, Surgery and Neurosciences, Diagnostic Imaging Unit, University of Siena, Siena, Siena, Italy
  12. 12Klinikum Vest Knappschaftskrankenhaus Recklinghausen, Department of Radiology and Neuroradiology, Recklinghausen, Germany
  13. 13Department of Advanced Biomedical Sciences, Ospedale Niguarda Ca Granda, Milano, Lombardia, Italy
  14. 14University Medical Center Hamburg-Eppendorf, Hamburg, Germany
  15. 15Eppdata GmbH, Hamburg, Germany
  16. 16Physiology, CURAM, University of Galway, Galway, Ireland
  17. 17Imaging Department, Imperial College Healthcare NHS Trust, London, UK
  1. Correspondence to Dr Kyriakos Lobotesis, Imaging Department, Imperial College Healthcare NHS Trust, London, UK; k.lobotesis{at}


Background A direct aspiration first pass technique (ADAPT) is an effective alternative to stent retriever thrombectomy for patients with large vessel occlusion (LVO). The PERFECT study evaluated direct aspiration with the EMBOVAC large bore aspiration catheter in patients with LVO strokes.

Methods PERFECT was a prospective, post-market, single-arm, multicenter, observational study of patients enrolled across 11 European centers between October 2020 and July 2022. Three direct aspiration passes with EMBOVAC were mandated before switching strategy. The primary endpoint was core-lab assessed successful reperfusion (modified Thrombolysis In Cerebral Infarction (mTICI) ≥2b) post-procedure. Other outcomes included first pass mTICI ≥2c, independent 90-day modified Rankin Scale (mRS) evaluation, and symptomatic intracerebral hemorrhage (sICH) at 24 hours by a clinical events committee.

Results EMBOVAC was used in 100 patients (mean age 70.4±14.0 years, 59.0% (59/100) female). Final mTICI ≥2b was achieved in 98.0% (97/99), final mTICI ≥2b with no change in frontline therapy or thrombolytics use during the procedure was achieved in 87.9% (87/99), final mTICI ≥2c in 86.9% (86/99), and first pass mTICI ≥2c in 53.5% (53/99). sICH at 24 hours was 0%. The 90-day mRS ≤2 rate was 56.6% (56/99) and all-cause mortality was 12.9%. One device-related serious adverse event occurred within 90 days (1.0%).

Conclusions PERFECT demonstrates that EMBOVAC achieves successful reperfusion rates and favorable clinical outcomes when used in the endovascular treatment of acute ischemic stroke (AIS) using a direct aspiration technique as first line therapy in a real-world setting in patients with AIS secondary to large vessel occlusion.

Trial registration Unique identifier: NCT04531904.

  • Stroke
  • Thrombectomy
  • Catheter
  • Device

Data availability statement

Data are available upon reasonable request.

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See:

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  • Direct aspiration is an alternative to stent retriever thrombectomy in patients with acute ischemic stroke (AIS) secondary to large vessel occlusion. EMBOVAC is a large bore aspiration catheter with an inner diameter of 0.071 inch. The PERFECT study assessed the safety and efficacy of EMBOVAC.


  • In the PERFECT multicenter, post-market observational study, direct aspiration with EMBOVAC as first line therapy resulted in high rates of successful mTICI ≥2b revascularization, fewer device passes, good clinical outcomes, and low complication rates.


  • The PERFECT study demonstrates the safety and effectiveness of EMBOVAC when used as first line therapy in a real-world, post-market European setting.


A direct aspiration first pass technique (ADAPT) with large bore aspiration catheters alone or combined with other mechanical thrombectomy (MT) techniques has been demonstrated to be safe and effective for treating acute ischemic stroke (AIS) secondary to large vessel occlusion (LVO).1–5 Three randomized controlled trials (RCTs) have compared the safety and effectiveness of direct aspiration versus stent retrievers: ASTER and Penumbra Separator 3D showed similar successful revascularization rates between techniques,1 3 and COMPASS demonstrated non-inferiority and shorter first pass recanalization time for aspiration compared with stent retrievers,5 supporting direct aspiration as an alternative to stent retriever as first line therapy.6

EMBOVAC (Cerenovus, Johnson & Johnson) is a large bore, single lumen, variable stiffness aspiration catheter with a 0.071 inch inner diameter, designed to aspirate emboli and thrombi in the neurovasculature either alone or in combination with stent retrievers. The Prospective Evaluation to Characterize the Real-World PerFormance of the EMBOVAC Aspiration Catheter for Neurothrombectomy: A Post-Market Clinical Follow-up Trial (PERFECT) study was conducted in Europe to assess the efficacy of EMBOVAC when used by multiple interventionalists and centers in AIS patients undergoing MT in a real-world clinical setting.


Study design

PERFECT was a prospective, multicenter, single-arm, post-market observational study, evaluating the safety and efficacy of endovascular clot removal with first line ADAPT using EMBOVAC for AIS. To minimize bias and variability, independent imaging core lab assessment (Eppdata, Hamburg, Germany), independent 90-day mRS assessment, and a clinical events committee were used.

Patient population

From October 2020 to May 2022, 100 consecutive AIS patients in 11 European sites were treated per investigator’s standard of care (SOC), with EMBOVAC mandated for the first three clot removal passes using ADAPT.4 Investigators enrolled eligible patients based on pre-specified inclusion and exclusion criteria (online supplemental table 1) after obtaining written informed consent.

Supplemental material


EMBOVAC is a large bore aspiration catheter with a 0.071 inch inner diameter designed to remove/aspirate neurovascular emboli/thrombi during AIS treatment. It consists of a single lumen, variable stiffness catheter with a braided reinforced shaft for support. A hydrophilic coating reduces friction during use. The catheter includes a distal radiopaque marker for angiographic visualization, a proximal luer hub for flushing and aspiration attachments, a hemostasis valve, and two peelable introducers. EMBOVAC is available in 125 cm and 132 cm usable length sizes.


Baseline data included medical history/demographic information, pre-stroke modified Rankin Scale (mRS) score, National Institutes of Health Stroke Scale (NIHSS) score, and CT/MRI data including initial Alberta Stroke Program Early CT Score (ASPECTS). Intravenous thrombolysis was administered according to standard guidelines in the absence of contraindication.

Patients underwent endovascular MT using EMBOVAC for the first three clot removal passes (if needed) for the target intracranial occlusion using ADAPT.4 Balloon guide catheter (BGC) use, anesthetic management, and any subsequent MT technique after three EMBOVAC passes were allowed at the operator’s discretion.

Patients were assessed 24 hours post-procedure for NIHSS, CT/MRI (independent imaging core lab), and reportable adverse events (AEs); 7 days post-procedure or discharge (−1/+7 days, whichever occurred first) for reportable AEs, NIHSS, and mRS scores if performed per SOC; and 90 days post-procedure for mRS scores (independent assessor), reportable AEs, and NIHSS scores if performed per SOC. Health economics data were collected during the procedure and each follow-up visit.

Outcome measures

The primary endpoint was end of procedure successful revascularization, defined as modified Thrombolysis In Cerebral Infarction (mTICI) ≥2b in the target vessel. Secondary efficacy outcomes included: (1) successful revascularization (final mTICI ≥2b) with no change in frontline therapy or use of thrombolytics during the procedure; (2) complete revascularization (final mTICI ≥2c); (3) first pass mTICI ≥2c; (4) first pass mTICI ≥2b; (5) time to recanalization (arterial puncture to mTICI ≥2b); and (6) 90-day mRS ≤2 (≥75 days). Revascularization was measured by the independent imaging core lab and reported using the expanded TICI (eTICI), inclusive of the 2c rating. For purposes of data comparisons, a minimum threshold of mTICI 2b was equal to eTICI 2b50.

Per the study protocol, during the first three passes of EMBOVAC operators were advised not to use rescue therapy, defined as: (1) any change in frontline device therapy to remove the target occlusion in a vessel ≥2 mm, (2) using intracranial stenting during the procedure, or (3) using an intra-arterial thrombolytic agent during the procedure (eg, tissue plasminogen activator (tPA), urokinase, pro-urokinase). Progression in therapy to address thrombus/occlusion that was no longer appropriate for EMBOVAC treatment (eg, using another device to remove distal occlusion in <2 mm vessel) was considered an appropriate evolution in SOC and not considered rescue therapy.

Safety outcomes included: (1) 90-day device-related serious adverse events (SAEs); (2) 24-hour symptomatic intracerebral hemorrhage (sICH) specified according to the Heidelberg Bleeding Classification,7 (3) 24-hour post-procedure NIHSS; and (4) 90-day all-cause mortality. SAEs were any adverse event that led to: (1) death; (2) serious deterioration in the health of the subject resulting in either a life-threatening illness or injury, permanent impairment of a body structure or function, including chronic diseases, in-patient or prolonged hospitalization, or medical/surgical intervention to prevent life threatening illness/injury or permanent impairment to a body structure or function; or (3) fetal distress, fetal death, or a congenital abnormality or birth defect.

Health economic-related endpoints included hospitalization length of stay (LOS) for the index procedure and unscheduled rehospitalizations and healthcare resource utilization for the index procedure. LOS in hospitalizations (days) was calculated as date of discharge−date of admission+1.

Statistical analysis

Descriptive summary statistics are presented for all endpoints. The number and percentage of subjects are summarized for categorical variables. Unless specified otherwise, percentages are based on subjects with non-missing values. Descriptive statistics for continuous variables include: number of subjects, mean, standard deviation (SD), median, first quartile (Q1), and third quartile (Q3). All statistical analyses were performed using SAS Studio, version 9.4.

Kaplan-Meier analysis (using product limit estimates) was applied to device-related SAEs and all-cause mortality. Kaplan-Meier event rate and its associated two-sided 95% confidence intervals (95% CI) using log-log transformation were reported. The estimate of standard error was computed using Greenwood’s formula. Subjects without events were censored at the date of last contact.

The modified intent-to-treat (mITT) analysis set included all enrolled subjects who received ≥1 EMBOVAC pass (defined as aspiration use followed by evaluation of revascularization with angiography). The mITT analysis set was used to analyze effectiveness endpoints. The safety analysis set included all enrolled subjects in whom treatment was attempted. The safety analysis set was used to analyze safety endpoints.

Subgroup analyses

The primary endpoint was analyzed by: (1) age at consent, (2) vascular location, (3) ASPECTS, (4) baseline NIHSS, (5) aspiration device position when aspiration started in pass 1, and (6) the system approach of using EMBOVAC in combination with CEREBASE using the mITT analysis set. Descriptive statistics for each subgroup were presented when there was a minimum of 10 subjects in all subgroup levels. Confidence intervals were not provided due to limited sample size.

A separate systems approach was used to assess the primary endpoint, and secondary effectiveness and safety endpoints of the mITT analysis set when treated with EMBOVAC in combination with the CEREBASE distal access guide sheath (CEREBASE, Cerenovus, Johnson & Johnson) in any pass, or with EMBOVAC in combination with a non-CEREBASE long sheath in any pass. CEREBASE was designed for use with EMBOVAC and is indicated for the introduction of interventional devices into the neurovasculature. It was designed for atraumatic vessel interaction with soft, compliant, and rounded distal edges and a highly flexible dexterous tip to minimize direct vessel wall contact. Descriptive statistics were presented based on observed data. Confidence intervals were not presented due to limited sample size.


Patient demographics and baseline characteristics

A total of 108 patients consented and 102 were enrolled. Online supplemental figure 1 shows the patient disposition flow chart. Demographic characteristics for the mITT and safety analysis sets are summarized in table 1. Mean age in the mITT group was 70.4±14.0 years, with over half of patients being female (59.0% (59/100)). The most common comorbidities were hypertension (65.0% (65/100)) and atrial fibrillation (43.0% (43/100)). Pre-stroke, most patients had an mRS of 0 (79.0% (79/100)) and an NIHSS ≥8 (86.0% (86/100)). A total of 72.0% (72/100) patients had a witnessed stroke with known onset date and time. Approximately half of patients received intravenous tPA at baseline (51.0% (51/100)). Baseline ASPECTS was 6–10 in 85.0% (85/100). Most occlusions were located in the middle cerebral artery-M1 segment 1 (71.0% (71/100)) and the internal carotid artery/carotid T (21.0% (21/100)). Demographic and baseline characteristics were similar in the safety analysis set.

Table 1

Patient demographics and baseline characteristics

Procedural characteristics

Procedural characteristics for both mITT and safety analysis sets are summarized in table 2. A total of 59.0% (59/100) mITT patients had general anesthesia. Mean time from symptoms onset to first aspiration attempt was 396.1±357.0 min, with 78.7% (74/94) patients having aspiration attempted ≤8 hours post-stroke. At least one stent retriever was used in 35.0% (35/100) and BGCs were used in 5.0% (5/100) patients. Mean number of total procedural passes was 2.4±2.2 (median (IQR) 1.0 (1.0–3.0)) and the maximum number of procedural passes for any subject was 11 (n=1). A total of 17.0% (17/100) patients were treated with another thrombectomy device at any pass (including a stent retriever combined with EMBOVAC). Within the first three passes of EMBOVAC, 10.0% (10/100) patients underwent either a change in frontline device therapy (7/10) and/or use of stenting (5/10) during the procedure. Procedural characteristics were similar for the safety analysis set. EMBOVAC use was unsuccessful in two patients due to vessel tortuosity.

Table 2

Procedural characteristics

Hospitalization analysis

Hospitalization analysis for the index procedure and unscheduled rehospitalizations for the mITT analysis set are summarized in online supplemental table 2. Median (IQR) total LOS was 8.0 (4.0–13.0) days and median LOS in the ICU was 3.0 (2.0–5.0) days. Patients with a total index LOS ≤2 days were likely transferred to another hospital. A total of 34.7% (33/95) patients were discharged home with self-care, 33.7% (32/95) discharged to other hospitals, and 24.2% (23/95) discharged to a rehabilitation center. A total of 12.6% (12/95) patients had at least one rehospitalization with a total of 14 rehospitalizations. Median LOS for rehospitalizations was 9.0 (8.0–20.0) days.

Efficacy and safety outcomes

Efficacy and safety outcomes are summarized in table 3. In the mITT analysis set, successful end-of-procedure mTICI ≥2b revascularization was achieved in 98.0% (97/99) of patients, with 87.9% (87/99) achieving successful procedural revascularization with no change in frontline therapy or use of thrombolytics during the procedure. A total of 86.9% (86/99) patients had complete procedural revascularization (final mTICI ≥2c), 53.5% (53/99) reached mTICI ≥2c following the first pass with EMBOVAC, and 72.7% (72/99) reached mTICI ≥2b following the first pass with EMBOVAC. Mean time to recanalization was 27.8±20.6 min and the 90-day mRS ≤2 rate was 56.6% (56/99). In the safety analysis set, the rate of device-related SAEs within 90 days was 1.0% (one patient with cerebral artery occlusion) and there were no instances of 24-hour sICH. Mean NIHSS at baseline was 14.8±6.4 and at 24 hours post-procedure was 8.0±6.4, with a mean change of −6.9±6.4. All-cause 90-day mortality was 12.9%.

Table 3

Efficacy and safety outcomes using EMBOVAC

Subgroup analysis

Online supplemental table 3 summarizes successful revascularization analyzed by subgroups, including patients aged ≤65 or >65 years, vascular location, ASPECTS (0–5, 6–7, and 8–10), baseline NIHSS <8 or >8, EMBOVAC used in combination with or without CEREBASE, and the aspiration device position <5 mm or >5 mm from the clot interface in the first pass. Outcomes were similar between each subgroup. In one subject, poor-quality images were not assessed by the core lab.

Systems approach

Online supplemental table 4 summarizes the safety and effectiveness endpoints in a subgroup of patients where EMBOVAC was used in combination with either CEREBASE (n=14) or other devices (n=51). The rate of successful revascularization (final mTICI ≥2b) when EMBOVAC was used in combination with CEREBASE (ie, no stent retriever used) in any pass was 100.0% (14/14) and with a non-CEREBASE long sheath was 98.0% (49/50). First pass mTICI ≥2c with no change in frontline therapy or use of thrombolytics during the procedure with CEREBASE was 85.7% (12/14) and with non-CEREBASE was 70.0% (35/50). Mean time to recanalization was 17.4 min with CEREBASE and 24.2 min with non-CEREBASE. The 90-day mRS ≤2 with CEREBASE was 78.6% (11/14) and with non-CEREBASE was 54.9% (28/51). The 90-day all-cause mortality was 0% with CEREBASE and 17.9% with non-CEREBASE.


PERFECT is the first clinical study of EMBOVAC characterizing the performance of EMBOVAC using ADAPT for AIS patients in a real-world, post-market clinical setting. EMBOVAC demonstrated high rates of successful mTICI ≥2b revascularization, few device passes, good clinical outcomes, and low complication rates, demonstrating the safety and effectiveness of EMBOVAC. Our systems approach analysis also demonstrated good angiographic and safety outcomes when EMBOVAC was used together with CEREBASE, supporting the use of these devices together.

Efficacy outcomes

PERFECT demonstrated high rates of final successful mTICI ≥2b revascularization with EMBOVAC used as a first-line contact aspiration approach, similar to studies with comparable patient populations. Three RCTs (ASTER,3 Penumbra Separator 3D,1 and COMPASS5) compared endovascular approaches of aspiration versus stent retriever thrombectomy. In ASTER, the rate of core lab-adjudicated successful end-of-procedure revascularization (mTICI ≥2b) after first-line contact aspiration was 85.4%.3 In Penumbra Separator 3D, mTICI ≥2b was achieved in 75.8% of patients per core lab.1 In COMPASS, TICI ≥2b at final assessment was achieved in 92% of patients who received aspiration first pass thrombectomy.5 Several meta-analyses have assessed successful revascularization rates with direct aspiration, including one specifically evaluating the efficacy of the SOFIA catheter, which reported mTICI ≥2b rates from 88.65–89%.8–10 Additionally, EMBOVAC had comparable rates of first pass mTICI ≥2b and mTICI ≥2c compared with a meta-analysis of nine studies using the SOFIA catheter for direct aspiration (first pass effect (FPE) 23.6%, modified FPE 36.1%),8 a meta-analysis by Arturo Larco et al11 of 13 studies assessing per-pass recanalization (FPE 32%, modified FPE 40%), COMPASS (modified FPE 57%),5 and a study by Baek et al12 assessing per-pass recanalization rates (modified FPE 45.3%). It is worth noting that, in PERFECT, 16% (16/100) of patients in the mITT and 16.7% (17/102) of patients in the safety analysis sets were treated without a microcatheter during the procedure, creating less than optimal support configuration, although good outcomes were still achieved with EMBOVAC.

Frontline therapy

Compared with applicable literature, successful revascularization rates without changing frontline therapy or using thrombolytics during the procedure in PERFECT are similar to the relevant RCTs, ranging from 63–83%.1 3 5 In ASTER, successful revascularization after first-line contact aspiration alone yielded an mTICI ≥2b rate of 63.0%.3 In Penumbra Separator 3D, mTICI ≥2b was achieved in 69.8% of patients who received aspiration alone.1 In COMPASS, rates of TICI 2b with the primary modality of aspiration first pass thrombectomy were 83%.5

Safety outcomes

The good functional outcome rate was higher in PERFECT compared with other studies. In the meta-analysis by Gory et al, the 90-day mRS ≤2 rate was 52.0%,10 and the meta-analysis by Phan et al13 reported 52.3%. The SOFIA meta-analysis reported a 90-day mRS ≤2 rate of 40.3%.8 The ASTER trial reported a 45.3% rate of 90-day mRS ≤2 for first-line contact aspiration,3 Penumbra Separator 3D reported 45.8% for patients treated with aspiration alone,1 and COMPASS reported 52% for aspiration first pass thrombectomy.5 These trials also had blinded mRS assessment. The 90-day all-cause mortality rate in PERFECT is comparable to or better than other published rates, including Gory et al (15.0%),10 Phan et al (12.5% for patients receiving ADAPT),13 ASTER (19.3% in patients with first-line contact aspiration),3 Penumbra Separator 3D (26.0% in patients receiving aspiration alone),1 COMPASS (22% in patients with aspiration first-pass thrombectomy),5 and the SOFIA meta-analysis (21.8%).8 There were no cases of sICH in PERFECT per independent clinical events committee adjudication of all ICH identified by the independent core imaging laboratory and a low procedural complication risk, supporting a good safety profile for EMBOVAC.


PERFECT was a single-arm study with no direct comparison to other devices. Independent imaging core laboratory and clinical outcome assessors were not blinded to device use because all patients used EMBOVAC. The independent imaging core laboratory was designed to mitigate potential site bias with an independent and standardized image assessment. The 90-day mRS assessors were required to be independent and not involved in previous assessments, treatments, or data entry for subjects. All safety endpoints were adjudicated by an independent clinical events committee, providing an impartial and standardized review of these events. PERFECT took place during the COVID-19 pandemic, which may have had an impact on the consistency of follow-up times and health of the patients, who are considered high risk for contracting COVID-19. The inclusion/exclusion criteria and the allowance of patient consent post-procedure introduces potential selection bias. Additionally, the small sample size limited subgroup and correlation analysis, restricting conclusions and generalizability.


The PERFECT study demonstrates that in the endovascular treatment of AIS using a direct aspiration technique, EMBOVAC achieves successful reperfusion with clinical outcomes comparable to those reported in the literature. The PERFECT study demonstrates that EMBOVAC is safe and efficacious in a real-world setting in patients with AIS secondary to large vessel occlusion.

Data availability statement

Data are available upon reasonable request.

Ethics statements

Patient consent for publication

Ethics approval

This study involves human participants and was approved by 1) CPP Nord-Ouest I (2021-A00659-32), 2) Ethik-Kommission der Ärztekammer Hamburg (2020-10052-BO-bet), 3) Ethik-Kommission der Christian-Albrechts-Universitat zu Kiel (D 516/20), 4) Ethik-Kommission der Medizinischen Fakultät der Ruhr-Universität Bochum (2020-724-b-S), 5) Ethik-Kommission der Ärztekammer Nordrhein (2021382), 6) Comitato Etico Univ. Cattolica del Sacro Cuore Policlinico Universitario Agostino Gemelli (3371), 7) Comitato Etico Milano Area 3 (343-18052022), 8) Comitato Etico Regione Toscana - Area Vasta Sud-Est (C.E.A.V.S.E.) (19941), 9) NRES Committee London - South East (20/LO/1111). Participants gave informed consent to participate in the study before taking part.


First, the authors would like to acknowledge Superior Medical Experts for editorial assistance. The authors would also like to acknowledge the contribution of the independent Clinical Events Committee members Chairperson Dr Heinrich Mattle (Department of Neurology, University of Bern), Dr Gerhard Schroth (Department of Interventional Neuroradiology, University of Bern), and Dr Mohamed Aggour (Department of Interventional Neuroradiology, The Royal London Hospital) for their assistance with study endpoints adjudication.


Supplementary materials

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  • Contributors MP, OJ: concept and design, data acquisition, critical revision of the manuscript for important intellectual content. GM, BG, HN, BE, AP, CC, CL, MZ, AS, AM: data acquisition, critical revision of the manuscript for important intellectual content. JF, KD: data acquisition, analysis, and interpretation, critical revision of the manuscript for important intellectual content. KL: guarantor, concept and design, data acquisition, analysis, and interpretation, manuscript drafting, critical revision of the manuscript for important intellectual content, supervision.

  • Funding The PERFECT study is sponsored by Cerenovus, Johnson & Johnson. Grant number: N/A.

  • Competing interests OJ: personal fees: Fa. Arcandis/Germany. GM: payment/honoraria for lectures, presentations, Speakers Bureaus, manuscript writing, educational events: Medtronic, Microvention; consulting fees: Stryker Neurovascular, Microvention Europe, Balt SAS, Sim and Size; paid lectures: Medtronic 675, Cerenovus, Bracco, Phenox. BG: consulting fees: Surge2surgery. HN: payment/honoraria for lectures, presentations, educational events: Acandis, Cerenovus, Phenox, Rapid medical. CC: payment/honoraria for lectures, presentations, Speakers bureaus, manuscript writing, educational events: Medtronic, Microvention, MIVI, Stryker. CL: proctoring/consultant services: Phenox; consultant services: Penumbra; travel and meeting expenses: Acandis, Penumbra; payment of honoraria for lectures and support for attending meetings: Phenox, Penumbra, Acandis. AS: employed by/holds shares: GSK. JF: research support: German Ministry of Science and Education, German Ministry of Economy and Innovation, German Research Foundation, European Union, Hamburgische Investitions-/ Förderbank, Medtronic, Microvention, Philips, Stryker; consultancy appointments: Acandis, Bayer, Boehringer Ingelheim, Cerenovus, Medtronic, Microvention, Penumbra, Phenox, Roche, Route92, Stryker, Tonbridge, TG Medical; stock holdings: Tegus Medical, Vastrax, Eppdata. KD: academic grants: Science Foundation Ireland. MP, BE, AP, MZ, AM, KL: nothing to disclose.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.