Real-World Study of Woven EndoBridge for Intracranial Aneurysm Treatment
Recruiting now
Conditions studied: Intracranial Aneurysm
In brief
We designed the Real-World Study of Woven EndoBridge for Intracranial Aneurysm Treatment (WEB-RWS), an ambidirectional, multicenter, post-market real-world study with a prospective active surveillance component. The study will include patients with IAs treated with commercially available WEB devices under the direction of treating physicians in routine clinical practice. Clinical, procedural, imaging, and safety data will be collected using a standardized electronic data capture system, with safety events adjudicated by an independent clinical events committee and imaging outcomes assessed by an independent core laboratory. The primary objective is to evaluate 12-month adequate aneurysm occlusion and major adverse events after WEB treatment. The study is expected to provide comprehensive post-market evidence on the real-world performance of the WEB device in China, including its safety, effectiveness, clinical appropriateness, and health economic value in routine neurointerventional practice.
Key facts
- Study ID
- NCT07620626
- Run by
- Xuanwu Hospital, Beijing
- People needed
- 1000
- Starts
- 2026-06-10
- Expected to finish
- 2028-06-30
- Last updated by the study team
- 2026-06-11
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Retrospective Cohort:
- Participants of any age and sex.
- Patients treated for an intracranial aneurysm using a commercially available MicroVention Woven EndoBridge device.
- Patients who completed at least one postoperative imaging follow-up.
- Prospective Cohort:
- Participants of any age and sex.
- Patients treated for an intracranial aneurysm using a commercially available MicroVention Woven EndoBridge device.
- The participant, or legally authorized representative if applicable, understands the study requirements and procedures and provides written informed consent before any study-specific data collection.
You may not qualify if…
- Retrospective Cohort:
- Patients treated with a Woven EndoBridge device for whom intraoperative or postoperative follow-up imaging data are not available.
- Patients considered by the investigator to be unsuitable for participation in this study.
- Prospective Cohort:
- Participants who are currently participating in, or plan to participate during the follow-up period, another clinical study that may affect the results of this study.
- Patients who are currently unable or expected to be unable to complete follow-up.
- Patients with a life expectancy of less than 1 year due to other diseases or conditions.
- Patients considered by the investigator to be unsuitable for participation in this study.
Where it is running
- Xuanwu Hospital — Beijing, China (enrolling)
Full record on ClinicalTrials.gov
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