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Intracranial Aneurysms clinical trials

View clinical trials related to Intracranial Aneurysms.

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NCT ID: NCT02312856 Completed - Clinical trials for Intracranial Aneurysms

Adjunctive Neurovascular Support for Wide-neck Aneurysm Embolization and Reconstruction

ANSWER
Start date: October 31, 2014
Phase: N/A
Study type: Interventional

This study is designed to evaluate the safety of the PulseRider in patients undergoing treatment for bifurcation basilar or carotid terminus aneurysms.

NCT ID: NCT02309203 Withdrawn - Clinical trials for Intracranial Aneurysms

Canadian Study of the MicroVention Flow Re-Direction (FRED) Endoluminal Device Stent System in the Treatment of Intracranial Aneurysms

CanFRED
Start date: n/a
Phase: N/A
Study type: Interventional

The study objective is to evaluate the safety and effectiveness of the MicroVention FRED System when used in the treatment of wide-necked intracranial aneurysms.

NCT ID: NCT02191618 Active, not recruiting - Clinical trials for Intracranial Aneurysms

The WEB-IT Clinical Study

WEB-IT
Start date: August 2014
Phase: N/A
Study type: Interventional

The study is a prospective, multicenter single-arm cohort. Patients with wide neck bifurcation aneurysms (WNBAs) have few choices for safe and effective endovascular treatment. In this study, all patients with qualifying WNBAs will be treated with the WEB. The primary effectiveness outcome of the study is the likelihood of complete intracranial aneurysm occlusion on the 1 year angiogram as adjudicated by a core laboratory.

NCT ID: NCT02125097 Completed - Clinical trials for Intracranial Aneurysms

The Reverse Barrel™ VRD Intracranial Aneurysm Trial

Barrel
Start date: December 1, 2013
Phase: N/A
Study type: Interventional

The purpose of this clinical investigation is to evaluate the safety and effectiveness of the Barrel™ VRD when used to facilitate endovascular coiling of wide-neck bifurcating or branch intracranial aneurysms with any approved embolic coils.

NCT ID: NCT02122133 Terminated - Clinical trials for Intracranial Aneurysms

CARE: A Prospective Multicenter Case Study to Assess Radiation Exposure in Patients Treated With the Penumbra Coil 400

CARE
Start date: May 2015
Phase:
Study type: Observational [Patient Registry]

The primary objective of this study is to gather data on the radiation exposure in patients treated with the Penumbra Coil 400™ System (PC 400) or conventional coils per their respective indications for use.This is a multicenter case review study of patients presenting with intracranial aneurysms who are treated with coil embolization therapy using the PC 400 or conventional coils. Data for each patient are collected acutely.Up to 90 patients treated with the PC 400 or conventional coils (2:1) at up to 15 centers in the USA will be enrolled.

NCT ID: NCT02066493 Active, not recruiting - Clinical trials for Intracranial Aneurysms

Giant Intracranial Aneurysm Registry

Start date: December 5, 2008
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to generate detailed insight into which therapies of giant intracranial aneurysms are being conducted, to document the natural history and the outcome of treatment over 5 years after inclusion into the Registry and to follow imaging data of giant aneurysms over years after diagnosis.

NCT ID: NCT02037932 Withdrawn - Aneurysm Clinical Trials

Hydrogel Balloon Assisted Intracranial Aneurysm Coiling Registry

GELATIN
Start date: January 2014
Phase: Phase 4
Study type: Interventional

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.

NCT ID: NCT01974700 Terminated - Seizures Clinical Trials

Seizure Prophylaxis in Aneurysm Repair

Start date: July 2013
Phase: Phase 4
Study type: Interventional

Seizures are a potential complication of surgical repair of intracranial aneurysms. In order to prevent seizures, many surgeons administer prophylactic anti-epileptic medication during the intra-operative and post-operative period, however, such practice is not supported by clinical data. Retrospective review found the incidence of postoperative seizures was higher in those who received anti-epileptics versus those who did not. The goal is to examine the utility of levetiracetam (Keppra) for seizure prophylaxis in patients undergoing surgical repair of unruptured intracranial aneurysms.

NCT ID: NCT01957683 Withdrawn - Clinical trials for Intracranial Aneurysms

Canadian eCLIPs™ Safety and Feasibility Study Protocol

CESIS
Start date: January 2020
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety and feasibility of the eCLIPs™ Family of Products for the treatment of unruptured intracranial bifurcation aneurysms in conjunction with embolization coils.

NCT ID: NCT01949779 Completed - Clinical trials for Intracranial Aneurysms

TransForm™ Occlusion Balloon Catheter Registry

Start date: December 2013
Phase:
Study type: Observational [Patient Registry]

The primary objective of this registry is to collect real world data on the safety and performance of the TransForm™ Occlusion Balloon Catheter when used in current neurointerventional procedures