Intra-arterial Neuroprotective Strategy for Ischemic STroke Patients With Endovascular Therapy (INSIST-ET)
Condition(s) studied
Investigational drug(s) / intervention(s)
Intra-arterial administration of neuroprotective agents: Intra-arterial administration of 3-n-butylphthalide for 16 to 24 hours during and after the operation at 17.36 to 26.04 ug/min
Study summary
To explore the safety and feasibility of intra-arterial neuroprotective strategy in acute ischemic stroke patients who received recanalization operation.
Eligibility
Primary outcome measure(s)
- Proportion of server adverse events — 48 hours
server adverse events including femoral artery dissection, local thrombosis, seudoaneurysm, arteriovenousfistula, etc.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Department of Neurology, General Hospital of Northern Theater Command | Shenyang | China | Recruiting |
More Hui-Sheng Chen trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04664933 on ClinicalTrials.gov ↗ ← All trials in China