Carotid Artery Stenting During Endovascular Treatment of Acute Stroke
Launched by UNIVERSITY MEDICAL CENTER GRONINGEN · Jul 15, 2024
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying whether performing a procedure called carotid artery stenting (CAS) right away during a treatment for acute stroke is safe and effective. The trial focuses on patients who have a specific type of stroke caused by a blockage in a large blood vessel in the brain and also have a significant narrowing or blockage in the carotid artery on the same side. The goal is to determine if treating the carotid artery at the same time as the stroke treatment can improve blood flow to the brain and reduce the risk of a second stroke, while also being mindful of potential risks like bleeding.
To participate in this trial, individuals must be at least 18 years old and have experienced an acute stroke related to a blockage in the main arteries supplying blood to the brain. They should also have a certain level of stroke severity as measured by a specific scale. Participants will be randomly assigned to either receive immediate stenting during their stroke treatment or to have their carotid artery problem treated later on. Throughout the trial, the researchers will keep track of how well the treatments work and whether they cause any complications. This trial is currently looking for volunteers and aims to provide important information about the best ways to treat strokes related to carotid artery issues.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Acute ischemic stroke due to proximal intracranial occlusion in the anterior circulation (intracranial ICA, M1, proximal M2) on the CT angiography
- • 2. Stenosis \>50% according to the NASCET criteria16 or initial occlusion of the ipsilateral cervical carotid artery of presumed atherosclerotic origin on baseline CT angiography
- • 3. Eligible for EVT according to the guidelines: EVT within 6 hours of onset or EVT between 6-24 hours after onset based on perfusion CT imaging selection (conform current guidelines)
- • 4. Baseline National Institute of Health Stroke Scale (NIHSS) score ≥2
- • 5. Age \>18 years
- • 6. Written informed consent (deferred consent)
- Exclusion Criteria:
- • 1. Any intracranial hemorrhage
- • 2. Cervical carotid artery stenosis or occlusion with other causes than presumed atherosclerosis (e.g. carotid artery dissection, floating thrombus, carotid web)
- • 3. Any exclusion criterion for EVT according to the guidelines
- • 4. Pre stroke disability (defined as a modified Rankin Scale score \>2)
- • 5. Recent gastro-intestinal or urinary tract hemorrhage (\<6 weeks)
- • 6. Recent severe head trauma (\<6 weeks)
- • 7. Recent infarction on baseline brain CT in the same vascular territory (\<6 weeks)
- • 8. Known allergy to aspirin and/or clopidogrel
- • 9. Pregnancy
About University Medical Center Groningen
University Medical Center Groningen (UMCG) is a leading academic medical center in the Netherlands, renowned for its commitment to innovative research, high-quality patient care, and extensive education in the medical field. As a prominent sponsor of clinical trials, UMCG leverages its multidisciplinary expertise and state-of-the-art facilities to advance medical knowledge and improve therapeutic outcomes. The center fosters collaboration among researchers, healthcare professionals, and industry partners, aiming to translate scientific discoveries into effective treatments that enhance patient health and well-being. With a focus on ethical standards and regulatory compliance, UMCG is dedicated to conducting clinical trials that contribute to the advancement of medicine and the betterment of society.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Groningen, , Netherlands
Patients applied
Trial Officials
Maarten Uyttenboogaart, MD PhD
Principal Investigator
University Medical Center Groningen
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported