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Clinical Trial Summary

This study employs a single-center, prospective, randomized controlled, double-blind exploratory research design. To investigate whether Sirolimus can reduce the rebleeding rate of brainstem cavernous malformations within 24 months after the first symptomatic bleeding event.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06091332
Study type Interventional
Source Huashan Hospital
Contact Zongze Li, Doctor
Phone +8613121226581
Email lizongze666@aliyun.com
Status Not yet recruiting
Phase Phase 2
Start date December 1, 2023
Completion date December 31, 2025