Trials / Recruiting
RecruitingNCT07135089
Improving Neuroprotective Strategy for Ischemic Stroke Before Endovascular Thrombectomy by Intravenous Tirofiban
Improving Neuroprotective Strategy for Ischemic Stroke Before Endovascular Thrombectomy by Intravenous Tirofiban (INSIST-IT2): a Prospective, Randomized, Double Blinded, Multi-center Study
- Status
- Recruiting
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 870 (estimated)
- Sponsor
- General Hospital of Shenyang Military Region · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
It remains uncertain whether intravenous tirofiban administered before endovascular thrombectomy could improve disability severity for patients with LVO due to intracranial atherosclerosis.The current study aimed to assess the efficacy and safety of administering intravenous tirofiban before endovascular thrombectomy for improving clinical outcomes in patients with anterior circulation LVO due to intracranial atherosclerosis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Intravenous tirofiban before endovascular thrombectomy | The tirofiban was administrated as a bolus dose of 10 μg/kg, followed by continuous infusion of 0.15 μg/kg/min for up to 24 hours. |
| DRUG | Intravenous placebo before endovascular thrombectomy | The placebo was administrated as a bolus dose of 10 μg/kg, followed by continuous infusion of 0.15 μg/kg/min for up to 24 hours. |
Timeline
- Start date
- 2025-11-13
- Primary completion
- 2027-09-30
- Completion
- 2027-12-30
- First posted
- 2025-08-21
- Last updated
- 2025-12-09
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT07135089. Inclusion in this directory is not an endorsement.