International Subarachnoid Aneurysm Trial II
Running, not enrolling · Not applicable
Conditions studied: Intracranial Hemorrhage Ruptured Aneurysm
In brief
The purpose of this study is to compare the clinical outcome of surgical clipping and endovascular coiling for ruptured intracranial aneurysms not included in the original ISAT Study.
Key facts
- Study ID
- NCT01668563
- Run by
- Centre hospitalier de l'Université de Montréal (CHUM)
- People needed
- 1724
- Starts
- 2012-11-12
- Expected to finish
- 2024-12-01
- Last updated by the study team
- 2024-08-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients at least 18 years of age
- At least one documented, intradural, intracranial aneurysm, ruptured within last 30 days
- SAH WFNS grade 4 or less
- The patient and aneurysm are considered appropriate for either surgical or endovascular treatment by the treating team
You may not qualify if…
- Patients with absolute contraindications administration of contrast material (any type)
- Patients with AVM-associated aneurysms
- Aneurysm located at basilar apex
Where it is running
- Montefiore Medical Center — The Bronx, New York, United States
- Foothills Medical Centre — Calgary, Alberta, Canada
- University of Alberta Hospital — Edmonton, Alberta, Canada
- Centre Hospitalier de l'Université de Montréal - Hôpital Notre Dame — Montreal, Quebec, Canada
- Vall d'Hebron Hospital — Barcelona, Spain
- University of Valladolid — Valladolid, Spain
Full record on ClinicalTrials.gov
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