Clinical trial Recruiting at 1 site Phase 3 Interventional Ages 18 and up

Intra-arterial Thrombolysis After Endovascular Thrombectomy in AIS

Official title: A Multicentre,Prospective,Randomized,Open Label,Blinded-endpoint Trial for Reperfusion Enhancement After Completing Thrombectomy Using Intraarterial Thrombolysis(REACT-IA-Thrombolysis Domain)Embedded in A Multi-faCtorial,mulTi-arm, Multi-staGe,Randomised,gLOBal Adaptive pLatform Trial for Stroke(ACT-GLOBAL) NCT06352632

Run by University of Calgary · NCT07687056 · Data updated 2026-11-12

This trial tests whether giving intra-arterial thrombolysis with tenecteplase or alteplase after endovascular thrombectomy helps improve recovery in adults with acute ischemic stroke.

Quick facts

PhasePhase 3
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment1500 (estimated)
SponsorUniversity of Calgary
Academic / other
Locations13 sites (Sydney, Barangaroo and 12 other locations)
StatusRecruiting
StartedAugust 11, 2026
Main results expectedDecember 31, 2030
Study endsMarch 31, 2031
Registry record updatedOctober 21, 2026
Trial IDNCT07687056 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 or older with acute ischemic stroke who undergo endovascular thrombectomy.

Probably not a fit

Patients who do not have distal occlusions or who are not suitable candidates for intra-arterial thrombolysis may see no benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a large, international, randomized trial embedded in the ACT-GLOBAL platform. It compares the use of intra-arterial thrombolytic therapy (tenecteplase or alteplase) versus no intra-arterial thrombolysis after endovascular thrombectomy in patients with acute ischemic stroke. The study uses a PROBE design with blinded outcome assessment and will enroll up to 1,500 participants, followed for 90 days. Randomization is stratified by country/region and thrombolytic agent to maintain balance across key covariates. Primary outcome is functional status at Day 90 measured by the modified Rankin Scale via centralized assessment.

Why it matters

Potential benefit: If successful, the approach could improve functional recovery for stroke patients who have distal occlusions after thrombectomy.

How similar studies have gone: Earlier small studies and meta-analyses have suggested safety and potential benefit with intra-arterial thrombolysis after thrombectomy, but definitive evidence has been lacking.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age ≥18 years
2. Clinical diagnosis of stroke

Exclusion Criteria:

There are no platform level exclusion criteria.

Where it's running

  • University of Calgary- Foothills Medical Centre
    Calgary, Alberta, Canada
    Recruiting
  • The George Institute for Global Health
    Sydney, Barangaroo, Australia
    Not yet recruiting
  • University of Alberta
    Edmonton, Alberta, Canada
    Not yet recruiting
  • Kelowna Regional Hospital
    Kelowna, British Columbia, Canada
    Not yet recruiting
  • Royal Columbian Hospital
    New Westminster, British Columbia, Canada
    Not yet recruiting
  • University of British Columbia
    Vancouver, British Columbia, Canada
    Not yet recruiting
Show 7 more locations
  • University of Manitoba - Winnipeg Health Science Centre
    Winnipeg, Manitoba, Canada
    Not yet recruiting
  • Health Sciences North Horizon Sante-Nord
    Greater Sudbury, Ontario, Canada
    Not yet recruiting
  • Ottawa Civic Hospital
    Ottawa, Ontario, Canada
    Not yet recruiting
  • Sunnybrook Health Science Centre
    Toronto, Ontario, Canada
    Not yet recruiting
  • CHUM -Centre Hospitalier de l'Universite de Montreal
    Montreal, Quebec, Canada
    Not yet recruiting
  • CIUSSS de l'Estrie - CHUS Fleurimont Hôpital (Sherbrooke)
    Sherbrooke, Quebec, Canada
    Not yet recruiting
  • Royal University Hospital
    Saskatoon, Saskatchewan, Canada
    Not yet recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.