GLPwatch

Glucagon-like Peptide-1 Receptor Agonists for Endovascular Stroke Thrombectomy

NCT07511543 · Not yet recruiting

Last updated 2026-07-27

This clinical trial is testing whether a type of diabetes medication called GLP-1 receptor agonists can help improve the success of a procedure to remove blood clots in people who have had an ischemic stroke.

Status Not yet recruiting Approved but enrollment has not started.
Phase Phase 3 Confirms effectiveness in a large group before approval.
Type Interventional (clinical trial)
Design Randomized, single-blind treatment study
Participants 826 people Planned (estimated).
Who can join Ages 18+ · all sexes
Timeline Started 2026-09 · est. completion 2031-12

What this study is testing ClinicalTrials.gov NCT07511543 ↗

Description as written by the study sponsor.

Endovascular thrombectomy (EVT) is a procedure that improves recovery for people who suffer from a stroke by removing blood clots from large blood vessels in the brain. However, even with this treatment, over half of the patients either pass away or are left with serious disabilities within three months. This is partly because, even in cases of a successful EVT, brain tissue damage continues to grow. Extent of brain damage is a major factor in how well a patient recovers. Studies in animals have shown that a drug called semaglutide might help protect the brain and improve recovery after a stroke. Semaglutide is currently used for the treatment of diabetes and obesity and is given as a weekly injection under the skin. The investigators are hoping to test whether giving semaglutide to stroke patients undergoing EVT can improve their recovery. A very large study at many hospitals is needed to answer this question. The investigators are starting with a vanguard phase of 100 patients with stroke who are scheduled for EVT in approximately 10 stroke centers across Canada. Once complete the full-scale phase III study of 826 patients (including 100 patients from the vanguard phase) at 52 global stroke centers will start. These patients will be randomly divided (like flipping a coin) into two groups: one will receive weekly semaglutide injections for 12 weeks, while the other will not receive the drug. During the vanguard phase, the investigators will track how many patients agree to participate, how many stay in the study, and how well they follow the treatment plan. The full trial will establish the benefit of semaglutide to improve the outcomes of patients with LVO treated with EVT.

Treatments tested

Main thing measuredVanguard phase: Feasibility - Recruitment
SponsorPopulation Health Research Institute
Conditions studiedIschemic Stroke
GLP-1 drugs

Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT07511543 ↗