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Clinical Trial Summary

The purpose of this study is to assess safety and effectiveness of the p64 MW HPC or p48 MW HPC Flow Modulation Device under prasugrel.


Clinical Trial Description

Title: Observational Registry With p64 MW HPC in Unruptured Anterior Circulation Aneurysms Under prasugrel Purpose: To assess safety and effectiveness of p64 MW HPC or p48 MW HPC under prasugrel in consecutive patients with unruptured anterior circulation aneurysms. Follow-up intervals: Independent follow-ups (after 3 to 6 months and after 12 months and after 24 months) according to site specific standard. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04305704
Study type Observational
Source Phenox GmbH
Contact Hans Henkes, Prof. Dr.
Phone +49 711 27834501
Email h.henkes@klinikum-stuttgart.de
Status Recruiting
Phase
Start date February 8, 2020
Completion date December 30, 2023

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