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Clinical Trial Summary

This study is a multicenter, prospective, open-label, endpoint-blind, randomized controlled study.Patients receiving surgical treatment for SICH were divided into groups using the random machine method. In addition to conventional treatment for spontaneous intracerebral hemorrhage, patients in the group of early initiation of antiplatelet therapy were given conventional dose of aspirin (100mg, qd) antiplatelet therapy starting from the 3rd day after surgery.An independent group of investigators evaluated cardiac, cerebral and peripheral vascular events and bleeding events at four different time points.To evaluate the benefits and safety of early postoperative initiation of antiplatelet therapy in patients with spontaneous intracerebral hemorrhage.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04820972
Study type Interventional
Source Beijing Tiantan Hospital
Contact JUN WU, MD
Phone +8613426322945
Email wujunslf@126.com
Status Recruiting
Phase N/A
Start date May 1, 2021
Completion date May 2023

See also
  Status Clinical Trial Phase
Recruiting NCT05232903 - Stromal Vascular Fraction (SVF) Therapy in Patients With Acute Spontaneous Intracerebral Hemorrhage (SICH). Phase 1
Recruiting NCT03862729 - Risk Stratification and Minimally Invasive Surgery in Acute ICH Patients
Completed NCT03183167 - Longitudinal Cohort Study on ICH Care N/A