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Clinical Trial Summary

The primary objective is to explore if HRS8179 could improve midline shift at 72 hours (or at time of decompressive craniectomy or comfort measures only, if earlier) in participants with large hemispheric infarction. The secondary objective is to explore if HRS8179 could improve acute neurologic status, functional outcomes, treatment requirements and safety.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05690711
Study type Interventional
Source Beijing Suncadia Pharmaceuticals Co., Ltd
Contact
Status Active, not recruiting
Phase Phase 2
Start date April 7, 2023
Completion date December 2024