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Clinical Trial Summary

To determine safety and occlusion rates when second-generation hydrogel coils are used in the treatment of ruptured intracranial aneurysms.


Clinical Trial Description

RAGE is a prospective, non-randomized, multicenter, post-market study. The RAGE study is designed to determine the safety and occlusion rates of hydrogel coils in the ruptured aneurysm study population. Secondary objectives include determining clinical outcomes, packing density, occlusion stability, rates of recurrence, rebleed, retreatment, and adverse events. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03252314
Study type Observational
Source Microvention-Terumo, Inc.
Contact Kellee Rivera, Semmes Murphey Foundation
Phone 901-260-6111
Email krrivera@semmes-murphey.com
Status Recruiting
Phase
Start date November 27, 2017
Completion date December 2025

See also
  Status Clinical Trial Phase
Recruiting NCT04391803 - EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysms With the Pipeline™ Flex Embolization Device With Shield TEchnology™ (ELEVATE) N/A
Terminated NCT02864940 - Memory Training in Aneurysmal Subarachnoid Hemorrhage Patients N/A
Active, not recruiting NCT03408379 - Impact of Platelet Activation in Intracranial Aneurysm Rupture Risk - PLAQRAN
Recruiting NCT04499508 - Appraising the Embolization of Aneurysms Using Balt Optima™ Coil System (APPLY Study) N/A