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Brain Aneurysm clinical trials

View clinical trials related to Brain Aneurysm.

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NCT ID: NCT04553549 Completed - Stroke, Acute Clinical Trials

Safety and Feasibility of the Infinity Catheter for Radial Access

Start date: October 1, 2020
Phase:
Study type: Observational

The main objective of this single arm study is to evaluate the safety and feasibility of the AXS Infinity LS (Stryker, Freemont, CA, USA) and AXS Infinity LS Plus (Stryker, Freemont, CA, USA) catheters during the transradial approach through a secondary use of the data collected during neurointerventional procedures. This includes evaluating the conversion rates to a transfemoral approach. A secondary aim of the study is to assess the radial artery occlusion rates post procedure.

NCT ID: NCT04439760 Completed - Brain Aneurysm Clinical Trials

Superior Cervical Ganglion Block, Transcranial Doppler

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to assess blood flow velocity in middle cerebral artery measured by transcranial doppler to determine the efficacy of SCG block in decreasing incidence or severity of vasospasm after MCA aneurysm surgery.

NCT ID: NCT03844334 Completed - Brain Aneurysm Clinical Trials

CLinical EValuation of WEB 0.017 Device in Intracranial AneuRysms

CLEVER
Start date: March 21, 2019
Phase:
Study type: Observational

The study is an observational, European, multi-center, prospective assessment of the clinical utility of the 0.017 WEB Aneurysm Embolization System in subjects with intracranial aneurysms deemed appropriate for endovascular treatment.

NCT ID: NCT02687607 Completed - Brain Aneurysm Clinical Trials

CLARYS: CLinical Assessment of WEB® Device in Ruptured aneurYSms

CLARYS
Start date: January 2016
Phase:
Study type: Observational [Patient Registry]

An observational non-randomized, multi-center, prospective assessment of the clinical utility of the WEB Aneurysm Embolization System in subjects with ruptured intracranial aneurysms deemed appropriate for endovascular treatment. The population being treated in this Registry is a subset of the CE marked indication.

NCT ID: NCT02435823 Completed - Brain Aneurysm Clinical Trials

Safety Study of the PulseRider® in Patients Undergoing Treatment for Bifurcation Intracranial Aneurysms

AWARD
Start date: March 31, 2015
Phase: N/A
Study type: Interventional

This is a prospective multi-center, single arm, non-randomized study. It is designed to evaluate the safety of the PulseRider® in patients undergoing treatment for bifurcation intracranial aneurysms.

NCT ID: NCT01975233 Completed - Brain Aneurysm Clinical Trials

WEB French Observatory of the WEB Aneurysm Embolization System

Start date: November 2012
Phase:
Study type: Observational

An observational post-market, open label, multicenter Observatory. The decision to use a WEB device to treat the patients has been made before and independently of the decision to include the patient in the French Observatory.

NCT ID: NCT01716117 Completed - Brain Aneurysm Clinical Trials

Safety and Effectiveness of an Intracranial Aneurysm Embolization System for Treating Large or Giant Wide Neck Aneurysms

SCENT
Start date: October 25, 2012
Phase: N/A
Study type: Interventional

This clinical research study is designed to determine safety and effectiveness of the Surpass Flow Diverter (Surpass System), an investigational device developed to treat wide-neck, large or giant intracranial aneurysms. An intracranial aneurysm is a bulge in the wall of a blood vessel in the brain. The bulge is caused by a weakening of the vessel wall. If left untreated, the bulge may continue to grow larger and ultimately the vessel may break open (rupture), resulting in serious bleeding into or around the brain. The information collected from this study will be used to evaluate how well patients do when treated with the Surpass System both immediately after treatment of an aneurysm and over a long period of time (5 years).

NCT ID: NCT01444664 Completed - Brain Aneurysm Clinical Trials

Aneurysm Wall Histology Registry

Start date: June 2010
Phase: Phase 4
Study type: Interventional

The purpose of this prospective registry is to determine if patients harboring intracranial aneurysms have any predictive markers between aneurysm wall tissue, cerebrospinal fluid and blood plasma.