Association Between a Peri-traumatic Dissociation State and the Occurrence of Post-traumatic Stress Syndrome

NCT ID: NCT03930966

Last Updated: 2022-01-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

148 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-04-09

Study Completion Date

2021-12-15

Brief Summary

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Patients will be selected after studying clinical records.Patients who had general anesthesia due to an injury related to severe trauma within 6 to 12 months prior to inclusion will be included.

Three self-survey will be completed by the patient: PDEQ, PCL-5 and a demographic questionnaire. According to the PDEQ and PCL-5 scores, an association between a peri-traumatic dissociation state and a post-traumatic stress disorder can be established.

Detailed Description

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Conditions

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Severe Trauma General Anaesthesia

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Prospective Study
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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PDEQ, PCL-5 and demographic survey

State of the patient evaluated with questionnaires to make the connection between peri-traumatic dissociation and the occurrence of post-traumatic stress disorder

Group Type EXPERIMENTAL

PDEQ, PCL-5 and demographic survey

Intervention Type DIAGNOSTIC_TEST

Questionnaires

Interventions

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PDEQ, PCL-5 and demographic survey

Questionnaires

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Patients with general anesthesia for a surgical wound with violent trauma in the road, a fall of more than 6 meters, burn, accident at work, explosion, aggression) in the 6 to 12 months before the inclusion
* Time between trauma and general anesthesia should not exceed 48 hours
* Patient agreeing to participate in the study.

Exclusion Criteria

* Minor patients
* Patients under curatorship, and tutorship
* Patient deprived of liberty
* Patients who do not speak French
* Patients who are not in satisfactory neurological state to answer the questionnaire (pyschotic, demented states)
* Patients who have been sedated (apart from general anesthesia) when receiving or having a Glasgow score \<14
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Brest

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Philippe ARIES, Dr

Role: PRINCIPAL_INVESTIGATOR

[email protected]

Locations

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CHRU Brest

Brest, , France

Site Status

Countries

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France

Other Identifiers

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DIStress-AG (29BRC18.0200)

Identifier Type: -

Identifier Source: org_study_id

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