Clinical Trials Directory

Trials / Completed

CompletedNCT04667637

Improving Neuroprotective Strategy for Ischemic Stroke With Sufficient Recanalization After Thrombectomy by Edaravone Dexborneol

Improving Neuroprotective Strategy for Ischemic Stroke With Sufficient Recanalization After Thrombectomy by Edaravone Dexborneol (INSIST-ED): a Prospective, Randomized, Double Blinded, Multi-centre Study

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
200 (actual)
Sponsor
Hui-Sheng Chen · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To explore the safety and efficacy of edaravone dexborneol for the treatment of acute ischemic stroke patients who received endovascular thrombectomy.

Conditions

Interventions

TypeNameDescription
DRUGedaravone dexborneolIntravenous injections of edaravone dexborneol (37.5mg, dissolved in 100ml saline) twice a day for 12 ±2 days.

Timeline

Start date
2021-02-23
Primary completion
2022-10-10
Completion
2022-10-10
First posted
2020-12-16
Last updated
2022-10-12

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04667637. Inclusion in this directory is not an endorsement.

Improving Neuroprotective Strategy for Ischemic Stroke With Sufficient Recanalization After Thrombectomy by Edaravone De (NCT04667637) · Clinical Trials Directory