Impact of Platelet Activation in Intracranial Aneurysm Rupture Risk - PLAQRAN

Sponsor
Fondation Ophtalmologique Adolphe de Rothschild (Other)
Overall Status
Recruiting
CT.gov ID
NCT03408379
Collaborator
(none)
230
1
179.4
1.3

Study Details

Study Description

Brief Summary

Sub arachnoid hemorrhage consecutive to intracranial aneurysm rupture is a devastating disease. Predictors of intracranial aneurysm rupture are limited and focus mainly on size and location. Platelet activation may have a deleterious role on aneurysm rupture. The assumption is that patients with ruptured intracranial aneurysm will present a higher rate of platelet activation compared to patients with non ruptured aneurysms.

Condition or Disease Intervention/Treatment Phase
  • Other: Collection of blood sample in aneurysm

Study Design

Study Type:
Observational
Anticipated Enrollment :
230 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Impact of Platelet Activation in Intracranial Aneurysm Rupture Risk - PLAQRAN
Actual Study Start Date :
Dec 20, 2017
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2032

Outcome Measures

Primary Outcome Measures

  1. Proportion of patients with platelet activation [in the 7 days before embolisation]

    comparison of this proportion between patients with ruptured versus non ruptured intracranial aneurysm

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient aged 18 and over

  • Patient presenting a single or multiple aneurysm

  • Patient presenting an intracranial aneurysm for which an intervention is planned (endovascular treatment or surgery) : elective intervention for an unruptured aneurysm or emergency surgery for a broken aneurysm

Exclusion Criteria:
  • Pregnant or breast feeding woman

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fondation Ophtalmologique A. de Rothschild Paris France 75019

Sponsors and Collaborators

  • Fondation Ophtalmologique Adolphe de Rothschild

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fondation Ophtalmologique Adolphe de Rothschild
ClinicalTrials.gov Identifier:
NCT03408379
Other Study ID Numbers:
  • MMI_2017_27
First Posted:
Jan 24, 2018
Last Update Posted:
Mar 14, 2022
Last Verified:
Mar 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Fondation Ophtalmologique Adolphe de Rothschild
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 14, 2022