Condition: Intracerebral Hemorrhage · Sponsor: National Taiwan University Hospital
This trial is a phase IIa human clinical study, in which 60 patients with intracerebral hemorrhage (ICH) at basal ganglion or thalamus within 6 h after onset will be enrolled. Patients will be randomly assigned as treatment group or control group as 1:1 distribution. Early initiation of celecoxib within 6 h after ICH and treatment for 21 days will be performed. The safety will be evaluated by drug adverse effects. The efficacy will be assessed by hematoma expansion, brain edema, and 3-month modified Rankin scale.
This description comes directly from the study's public registry record.
Shin-Joe Yeh, MD PhD · 886-2-23123456 · shinjoeyeh@gmail.com
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| Natinal Taiwan University Hospital | Taipei, Taiwan | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05434065