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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04078789
Other study ID # APHP190619
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 2022
Est. completion date September 2024

Study information

Verified date March 2022
Source Assistance Publique - Hôpitaux de Paris
Contact Céline Dufort, MD
Phone +33147107698
Email céline.durfort@aphp.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main objective of this study is to describe the care pathway of patients presenting in the medico-judicial unit of the Raymond Poincaré Hospital in Garches, France, following a complaint for sexual assault and suggest ways to improvement of the care adapted to the characteristics of the participants.


Description:

AS secondary objectives, the study aims to: - Analyze the population of victims of sexual assault seen in consultation at the medico-judicial unit of Raymond Poincaré Hospital. - Analyze the decision elements of the initiation of the post-exposure treatment and evaluate them against the recommendations. - Analyze the data collected on the patients and their follow-up in consultation of infectious disease of the hospital of Garches following a sexual assault. - Identify obstacles encountered by participants to follow the complete follow-up path. For this purpose the data collection will be done initially within the forensic unit of Raymond Poincaré Hospital. Then, in a second step, the patients requiring the setting up of a post-exposure treatment, are addressed in the service of infectious diseases. The compilations of the data necessary for the study will then be continued until 3 months after the sexual assault. For the collection of data, they will be based on the medical records of the victims.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 250
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender All
Age group N/A to 120 Years
Eligibility Inclusion Criteria: - People declared being victim of sexual assault; - Consult at medical-legal unit; - Judicial requirement. Exclusion Criteria: - Absence of judicial requirement.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Outcome

Type Measure Description Time frame Safety issue
Primary post-exposure prophylaxis requirement and surveillance termination Prevalence of a consultant victim at the medico-legal unit, requiring post-exposure prophylaxis and completing their post-sexual assault surveillance. at 1 year
Secondary Consulting at the medico-legal unit Description of victims consulting at the medico-legal unit. at 1 year
Secondary Follow-up in medico-legal unit Follow-up of the start of the post-exposure prophylaxis: indication, difficulty of the prescription, respect of the recommendations. at 1 year
Secondary Follow-up in the infectious diseases department Description of the patients followed in the department of acute medicine specializing in infectious diseases sent by the medico-legal unit following sexual assault: monitoring of sexually transmitted infections, aspects of psychological care, state of coverage vaccine, rate of completion, causes of cessation of the treatment, reasons for the failure of follow-up. at 1 year
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