Condition: Intracranial Arterial Stenosis · Brain Diseases · Sponsor: The Affiliated Hospital of Qingdao University
This clinical trial is a prospective, multicenter, single-arm study. About 300 subjects undergoing rapamycin-eluting stent implantation will be enrolled based on the inclusion and exclusion criteria. The primary endpoint is the rate of any stroke or death within 1 month. Secondary efficacy endpoints include immediate stent implantation success. Safety endpoints cover the incidence of stroke or neurological death, target-vessel-related stroke or death, all-cause mortality, and mRS scores at 12-month follow-ups. Subjects will be clinically followed up before surgery, device implantation, discharge, and at 1, 6, and 12 months post-surgery. An imaging subgroup of at least 80 subjects who agree to DSA follow-up at 12 months will assess in-stent restenosis (\>50%).
This description comes directly from the study's public registry record.
Yong Zhang · (+86) 18661818866 · bravezhang@126.com
Always discuss trial participation with your own doctor first.
| Qingdao University Affiliated Hospital | Qingdao, Shandong, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07352852