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Clinical Trial Summary

The aim of the study is to demonstrate a significant improvement in quality of life specific to patients with fibromyalgia syndrome in patients with fibromyalgia syndrome with comorbid posttraumatic stress disorder, treated with reconsolidation blockade. Patients receive a treatment with propranolol associated with reconsolidation blockade of traumatic story once a week during 6 weeks, with evaluation at inclusion and at 3 months.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04950426
Study type Interventional
Source Centre Hospitalier Henri Laborit
Contact Nematollah JAAFARI, Professor
Phone 0033 5 16 52 61 18
Email namatollah.jaafari@ch-poitiers.fr
Status Recruiting
Phase Phase 2
Start date August 13, 2021
Completion date August 12, 2024

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