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Clinical Trial Summary

Rationale: Intrasaccular neck occlusion devices have been used for unruptured aneurysm without safety concerns and good occlusion rates. In the setting of a subarachnoid hemorrhage, they could improve the rate of complete occlusion without safety concerns. Aim: To explore the safety and efficacy of intrasaccular neck occlusion devices in patients with acute subarachnoid hemorrhage caused by a ruptured saccular aneurysm by a one arm prospective registry. Study outcome: The primary outcomes is the rate of complete occlusion (Raymond-Roy I) and rebleeding at one year follow-up. The primary safety outcome is rate of rebleeding during the admission.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05171465
Study type Observational [Patient Registry]
Source Hospital Universitari Vall d'Hebron Research Institute
Contact Alejandro Tomasello, MD
Phone 934893000
Email alejandrotomasello@gmail.com
Status Not yet recruiting
Phase
Start date March 2022
Completion date March 2024

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