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CompletedNCT02814409

Alteplase-Tenecteplase Trial Evaluation for Stroke Thrombolysis

Alteplase-Tenecteplase Trial Evaluation for Stroke Thrombolysis (ATTEST 2)

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
1,858 (actual)
Sponsor
NHS Greater Glasgow and Clyde · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The principle research question is: in patients with acute ischaemic stroke eligible for intravenous (IV) thrombolysis, is tenecteplase superior in efficacy to alteplase, based on functional outcome as assessed by modified Rankin Scale distribution at day 90?

Conditions

Interventions

TypeNameDescription
DRUGIntravenous recombinant tissue plasminogen activator (rtPA) AlteplaseIV Alteplase 0.9mg/kg (max 90mg) bolus + 1h infusion
DRUGIntravenous TenecteplaseIV Tenecteplase 0.25mg/kg (max 25mg) single bolus

Timeline

Start date
2016-12-15
Primary completion
2023-08-31
Completion
2024-01-10
First posted
2016-06-27
Last updated
2024-06-13

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02814409. Inclusion in this directory is not an endorsement.

Alteplase-Tenecteplase Trial Evaluation for Stroke Thrombolysis (NCT02814409) · Clinical Trials Directory