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Repetitive Transcranial Magnetic Stimulation Plus Reactivation Therapy Efficacy on PTSD Symptom Severity in Resistant PTSD - Trial NCT06111976

Access comprehensive clinical trial information for NCT06111976 through Pure Global AI's free database. This phase not specified trial is sponsored by Assistance Publique - Hรดpitaux de Paris and is currently Not yet recruiting. The study focuses on Post Traumatic Stress Disorder. Target enrollment is 102 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT06111976
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Trial Details
ClinicalTrials.gov โ€ข NCT06111976
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Repetitive Transcranial Magnetic Stimulation Plus Reactivation Therapy Efficacy on PTSD Symptom Severity in Resistant PTSD
Repetitive Transcranial Magnetic Stimulation Plus Reactivation Therapy Efficacy on PTSD Symptom Severity in Resistant PTSD, a Randomized Double Blind Sham Controlled Trial (TraumaStim)

Study Focus

Repetitive Transcranial Magnetic Stimulation (rTMS)

Interventional

procedure

Sponsor & Location

Assistance Publique - Hรดpitaux de Paris

Paris, France

Timeline & Enrollment

N/A

Dec 01, 2023

Jul 01, 2026

102 participants

Primary Outcome

PTSD severity score measured at M1 after 12 sessions of rTMS or sham rTMS and simultaneous reactivation of traumatic memory

Summary

A French multicenter randomized and double blinded shamed controlled study recruiting
 patients who present resistant PTSD. The aim of this trial is to assess the efficacy of
 cerebral modulation by rTMS with simultaneous reactivation of traumatic memory on the PTSD
 symptoms at M1.

ICD-10 Classifications

Post-traumatic stress disorder
Traumatic shock
Personal history of psychological trauma, not elsewhere classified
State of emotional shock and stress, unspecified
Neurotic, stress-related and somatoform disorders

Data Source

ClinicalTrials.gov

NCT06111976

Non-Device Trial