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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


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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