Actively Recruiting
Evaluation of Functional Recovery of Patients With Acute Ischemic Stroke Treated by Thrombectomy
Led by University Hospital, Montpellier · Updated on 2024-05-28
540
Participants Needed
1
Research Sites
178 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The management of cerebral infarctions (CI) is a real public health issue. The French National Authority for Health recommends Mechanical Thrombectomy (MT) either in combination with Intravenous Thrombolysis (IVT), or alone, after failure of IVT or in case of contraindication to IVT, within 6 hours of the onset of symptoms. The objective is to determine the factors predicting good functional recovery at 3 months in order to establish the typical profile of the "good responder" patient to MT and to evaluate functional recovery at 3 and 12 months (mRS ≤ 2) according to the modality of MT (depending on whether it is performed during the day or at night), the age of the patients, the equipment used for MT, the type of anaesthesia, as well as the impact of the metrics from the radiological evaluation in the patient's management. patient management.
CONDITIONS
Official Title
Evaluation of Functional Recovery of Patients With Acute Ischemic Stroke Treated by Thrombectomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Indication for treatment with Mechanical Thrombectomy
- Imaging on admission showing occlusion of a large intracranial artery (anterior, middle, posterior cerebral artery, basilar artery, vertebral artery)
- Health insurance coverage
- Obtaining the patient's consent
You will not qualify if you...
- Serious intercurrent illness impacting short-term survival and preventing 3-month follow-up
- Inability to complete follow-up (e.g., foreign tourists)
- Legal incapacity (under guardianship, curatorship, or deprived of liberty)
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University Hospital of Montpellier
Montpellier, France, 34295
Actively Recruiting
Research Team
C
Cyril Dargazanli
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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