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Clinical Trial Summary

The aim of this study is to demonstrate the effectiveness of propranolol in blocking reconsolidation by reducing PTSD symptoms in the short and long term in adolescents with PTSD for more than 3 months.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04921982
Study type Interventional
Source Rennes University Hospital
Contact Jacques Dayan, Pr
Phone 299284321
Email jacques.dayan@chu-rennes.fr
Status Not yet recruiting
Phase Phase 2
Start date May 2023
Completion date June 2026

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