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Study identifier: NCT04686877 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Safety and Efficacy of Stereotactic Aspiration Plus Urokinase in Deep Intracerebral Hemorrhage Evacuation

Condition: Treatment of Spontaneous Intracerebral Hemorrhage  ·  Sponsor: First Affiliated Hospital of Fujian Medical University

PhaseNA
Planned participants400
Who can joinAll sexes, 40 Years to no upper limit
Healthy volunteersNo

About this study

This is a nationwide, multicenter, open-label, randomized controlled trial of early minimally invasive treatment for deep-seated spontaneous cerebral hemorrhage (dICH). The study consists of 2 steps: the first step is to conduct a dose climbing test to determine the safety and optimal dose of urokinase intra-hematoma irrigation after stereotactic aspiration; the second step is to validate whether stereotactic aspiration plus urokinase irrigation (the optimal dose determined in step one) is superior to conservative treatment in improving long-term outcomes (1 year) in early (within 24h) dICH patients.

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

Talk to the study team

Lin Fuxin, PHD,MD  ·  +86 13552358381  ·  lfxstuy@126.com

Kang Dezhi, MD  ·  +86 13859099988  ·  kdz999888@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

First Affiliated Hospital of Fujian Medical UniversityFuzhou, Fujian, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT04686877