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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05471895
Other study ID # 2021/CHU/28
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 2023
Est. completion date June 2023

Study information

Verified date July 2022
Source Centre Hospitalier Universitaire de la Réunion
Contact Aïda Rakotoarinosy
Phone 02 62 35 90 00
Email rkt.aida@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

According to the figures for the last three years collected from the Indian Ocean Regional Health Observatory, it appears to be about twice as many voluntary terminations of pregnancy on the island of Reunion compared with France metropolitain region. Furthermore, the overseas section in 2002, which looked at violence against women of all types in three different spheres of life (the marital sphere, the workplace and public spaces), tends to show a much higher incidence of sexual violence than in metropolitain France. This trend seems to be confirmed by the overseas section of the VIRAGE survey started in 2018 on the island. Furthermore, data found in a qualitative study conducted in Ile de France in 2013 seems to demonstrate a more frequent use of abortion among patients who are victims of sexual violence. Thus, thiçs study will consist in evaluating the impact of sexual violence on the incidence of voluntary termination of pregnancy in Reunion Island.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 1000
Est. completion date June 2023
Est. primary completion date April 2023
Accepts healthy volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patient coming for an abortion request at the CHU SUD and NORD, at the GHER and at the CEPS for the CHOR (Reunion Island) Exclusion Criteria: - Patient coming to the above-mentioned centres for a "post-abortion" consultation. - <18 years - Patient who does not speak French. - Illiterate patient. - Patient who has already completed the questionnaire. - Patient refusing to participate in the study.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de la Réunion

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of women victims of sexual abuse coming for a voluntary termination of pregnancy Number of patients coming for a voluntary termination of pregnancy sexually abused Day 1
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