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Advancing Stroke Safety and Efficacy Through Early Tirofiban Administration After Intravenous Thrombolysis (ASSET-IT) - Trial NCT06134622

Access comprehensive clinical trial information for NCT06134622 through Pure Global AI's free database. This Phase 3 trial is sponsored by The First Affiliated Hospital of University of Science and Technology of China and is currently Not yet recruiting. The study focuses on Acute Ischemic Stroke. Target enrollment is 832 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT06134622
Phase 3
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06134622
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Advancing Stroke Safety and Efficacy Through Early Tirofiban Administration After Intravenous Thrombolysis (ASSET-IT)

Study Focus

Acute Ischemic Stroke

Intravenous thrombolysis plus tirofiban

Interventional

drug

Sponsor & Location

The First Affiliated Hospital of University of Science and Technology of China

Hefei, China

Timeline & Enrollment

Phase 3

Jan 01, 2024

Jun 30, 2027

832 participants

Primary Outcome

a modified Rankin Score of 0-1

Summary

To assess the efficacy and safety of tirofiban administration after intravenous thrombolysis
 for patients with AIS.

ICD-10 Classifications

Stroke, not specified as haemorrhage or infarction
Sequelae of stroke, not specified as haemorrhage or infarction
Cerebral infarction
Cerebral infarction, unspecified
Transient cerebral ischaemic attack, unspecified

Data Source

ClinicalTrials.gov

NCT06134622

Non-Device Trial