Trials / Completed
CompletedNCT04086147
CHinese Acute Tissue-Based Imaging Selection for Lysis In Stroke -Tenecteplase
Chinese Acute Tissue-based Imaging Selection for Lysis in Stroke: a Prospective, Multicentre, Randomized, Open-label, Rater-blinded, Randomized Trial
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 86 (actual)
- Sponsor
- Huashan Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To select the best dosage of tenecteplase for acute ischemic stroke patients (onset time 4.5-24h) of large vessel occlusion using early combined CT/MR imaging outcomes
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Low dose tenecteplase | Intravenous (IV) tenecteplase 0.25 mg/kg (single bolus; maximum dose 25 mg) |
| DRUG | High dose tenecteplase | Intravenous (IV) tenecteplase 0.32 mg/kg (single bolus; maximum dose 32 mg) |
Timeline
- Start date
- 2019-12-09
- Primary completion
- 2021-12-31
- Completion
- 2021-12-31
- First posted
- 2019-09-11
- Last updated
- 2022-03-31
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT04086147. Inclusion in this directory is not an endorsement.