Reducing Reconsolidation of Trauma Memories With Propranolol

Status Recruiting

Clinical Trial Summary

The purpose of this study is to test whether propranolol is capable of reducing subsequent physiological trauma-related conditioned responses, as well as self-reported post-traumatic stress disorder (PTSD) symptoms.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01349439
Study type	Interventional
Source	Douglas Mental Health University Institute
Contact	Alain R Brunet, Ph.D.
Phone	514-761-6131
Email	alain.brunet@mcgill.ca
Status	Recruiting
Phase	Phase 2
Start date	March 2011

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