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NCT02879175 Clinical Trial

Patients' Follow-up After Subarachnoid Haemorrhage Caused by Ruptured Intracranial Aneurysms

Intracranial Aneurysms Clinical Trial

— FUSAC  

Official title:
Patients' Follow-up After Subarachnoid Haemorrhage Caused by Ruptured Intracranial

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT02879175
Other study ID # RBC_2016_9
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date September 8, 2016
Est. completion date September 2031

Study information
Verified date September 2023
Source Fondation Ophtalmologique Adolphe de Rothschild
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

After endovascular treatment of the intracranial aneurysm, recanalization may occur, with a risk of recurrent subarachnoid haemorrhage or long-term angiographic recurrences of aneurysms. Few data exist on patients' long-term follow-up after subarachnoid haemorrhage caused by ruptured intracranial aneurysms.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 400
Est. completion date September 2031
Est. primary completion date September 2031
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Subarachnoid haemorrhage caused by ruptured intracranial aneurysms - endovascular embolization of the aneurysm Exclusion Criteria: - none

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Fondation Opthalmologique A de Rothschild Paris

Sponsors (1)
Lead Sponsor Collaborator
Fondation Ophtalmologique Adolphe de Rothschild

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary early neurological clinical recovery modified Rankin scale 1 year after Subarachnoid Haemorrhage
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