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Hydrogel Balloon Assisted Intracranial Aneurysm Coiling Registry — GELATIN  

Aneurysm Clinical Trial

Official title:
Hydrogel Balloon Assisted Intracranial Aneurysm Coiling Registry

Clinical Trial Summary

The objective of the GELATIN registry is to prospectively evaluate intracranial aneurysm occlusion and retreatment rates as well as adverse event rates in patients undergoing balloon-assisted coiling using the MicroVention Scepter Occlusion Balloon Catheter and second-generation MicroVention hydrogel coils for treatment of previously treated or untreated ruptured and unruptured intracranial aneurysms.

Clinical Trial Description

This is a prospective, single arm, single center study of patients with ruptured or unruptured saccular aneurysms that are embolized using MicroVention second-generation hydrogel coils and undergo balloon remodeling with the MicroVention Scepter Occlusion Balloon Catheter. Data for each patient will be collected 6 ± 3 months post-procedure for the study. ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02037932
Study type Interventional
Source Medical College of Wisconsin
Contact
Status Withdrawn
Phase Phase 4
Start date January 2014
Completion date June 2017
View Details
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