Clinical Trials Directory

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

TypeNameDescription
DRUGLow dose tenecteplaseIntravenous (IV) tenecteplase 0.25 mg/kg (single bolus; maximum dose 25 mg)
DRUGHigh dose tenecteplaseIntravenous (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.

CHinese Acute Tissue-Based Imaging Selection for Lysis In Stroke -Tenecteplase (NCT04086147) · Clinical Trials Directory