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

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorPopulation Health Research Institute

About this trial

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 smaller study to gain information on whether it is possible to perform a larger definitive one, and if so, how best to plan for it. In this first step the investigators will study 100 patients with stroke who are scheduled for EVT in approximately 10 stroke centers across Canada. 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. 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 investigators will also monitor the patients' recovery, overall health, and any side effects from the treatment. These results will provide important information to plan the larger study with the goal of reducing death rates and long-term disability in stroke patients undergoing EVT.

Eligibility criteria

Qualifiers

Age 18 years or above on the date of randomization.

EVT for an LVO in the anterior circulation, defined as the intracranial segment of the internal carotid artery (ICA) and/or the M1 or proximal M2 segment of the middle cerebral artery (MCA).

National Institutes of Health Stroke Scale (NIHSS) ≥ 6 points at the time of randomization.

Pre-stroke modified Rankin Scale (mRS) 0 or 1.

Disqualifiers

Pregnancy or breast-feeding.

Renal insufficiency (creatinine clearance < 30mL/min).

Cirrhosis or severe hepatic dysfunction, characterized by jaundice, encephalopathy or coagulopathy.

History of pancreatitis in the year prior to randomization or evidence of acute pancreatitis on randomization.

Trial design

Treatments tested in this trial

  • Semaglutide

Treatment groups

100 Participants
are divided into 2 treatment groups

Locations

This trial has no locations