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Study identifier: NCT07707076 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Flow Diverter Versus Conventional Endovascular Treatment for Unruptured Wide-Neck Bifurcation Aneurysms (FD-BWA Trial)

Condition: Unruptured Intracranial Wide-neck Bifurcation Aneurysms  ·  Sponsor: Nanfang Hospital, Southern Medical University

PhaseNA
Planned participants266
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Brief Summary: The goal of this clinical trial is to compare whether the traditional approach (stent-assisted coiling) is associated with a lower complication rate than flow diverter (Pipeline™) treatment for unruptured intracranial wide-neck bifurcation aneurysms. It will also evaluate the long-term imaging outcomes and safety of both treatments. The main questions it aims to answer are: * Does the traditional approach result in a lower rate of any stroke or all-cause death within one year after treatment compared to the flow diverter? * What medical problems do participants experience during and after each treatment? * What are the imaging cure and stability rates at 1, 2, and 5 years after treatment? Researchers will compare the traditional approach (stent-assisted coiling) with the flow diverter (Pipeline™) to determine which treatment has better safety and efficacy outcomes. Participants will: * Be randomly assigned to receive either the flow diverter or traditional stent-assisted coiling * Undergo the assigned endovascular procedure * Return for follow-up visits at 30 days, 6 months, 1 year, 2 years, and 5 years after surgery for clinical assessments and imaging examinations (DSA, MRA, or CTA)

This description comes directly from the study's public registry record.

Talk to the study team

Huibin Kang, MD  ·  +8602062787842  ·  kanghuibindoctor@163.com

Wenfeng Feng, MD  ·  +8602062787665  ·  fengwf1967@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Nanfang Hospital, Southern Medical UniversityGuangzhou, Guangdong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07707076