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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04379648
Other study ID # 10477M-TEDI
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 5, 2019
Est. completion date September 5, 2021

Study information

Verified date May 2020
Source Centre hospitalier de Ville-Evrard, France
Contact BENCHERIF Youcef, CRA
Phone 0143093030
Email y.bencherif@epsve.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

More than 70% of ambulatory patients with IDD have attempted suicide (APA, 2015). This disorder, as well as all the disorders on the dissociation spectrum, must therefore be clarified and better diagnosed.

The goal of this research is :

1. to assess the prevalence of dissociative disorders using specific tools in patients suffering from PTSD.

2. to validate the French version of the DDIS interview (Ross, 1997) that the investigators have translated.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date September 5, 2021
Est. primary completion date September 5, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient diagnosed with PTSD according to DSM 5 criteria

- Over 18 years of age

- Informed consent signed

Exclusion Criteria:

- Neurological disorders

- Serious and/or unstable somatic pathologies

- Patient not affiliated with social security

- Patient hospitalized under restraint in psychiatric care by decision of the state representative or in psychiatric care at the request of a third party

- Patient under guardianship

- Patient participating in parallel in another biomedical research

- Change of antidepressant in the last three months

- Patient not mastering the French language

Study Design


Intervention

Other:
self-assessment and hetero-assessment
Self assessment for the passing of the following rating scales CTQ-SF36-ITQ-PCL5-DES Hetero-assessment for the pasing of the following rating scales DDIS FR and medical interview

Locations

Country Name City State
France Youcef BENCHERIF Neuilly Sur Marne Île De France

Sponsors (1)

Lead Sponsor Collaborator
Januel

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Post Traumatic Stress assessment of the prevalence of dissociative disorders in a cohort of patients with PTSD 1 year
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