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Trials / Completed

CompletedNCT05395338

1-year Clinical Outcomes in Recombinant Tissue Plasminogen Activator (Rt-PA) Treated Chinese Acute Ischaemic Stroke (AIS) Patients

1-year Clinical Outcomes After Intravenous Rt-PA for Chinese AIS Patients

Status
Completed
Phase
Study type
Observational
Enrollment
12,551 (actual)
Sponsor
Boehringer Ingelheim · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of the study is to find out the 1-year clinical outcomes among Acute Ischaemic Stroke (AIS) patients who were treated with intravenous (IV) Recombinant Tissue Plasminogen Activator (rt-PA) within 4.5 hours of symptom onset compared with those who arrived or were admitted to the hospital within 4.5 hours of symptom onset and did not receive any reperfusion treatment in a real-world clinical setting.

Conditions

Interventions

TypeNameDescription
DRUGrt-PARecombinant Tissue Plasminogen Activator

Timeline

Start date
2022-04-12
Primary completion
2022-11-30
Completion
2022-11-30
First posted
2022-05-27
Last updated
2024-10-16
Results posted
2024-10-16

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05395338. Inclusion in this directory is not an endorsement.

1-year Clinical Outcomes in Recombinant Tissue Plasminogen Activator (Rt-PA) Treated Chinese Acute Ischaemic Stroke (AIS (NCT05395338) · Clinical Trials Directory