The Use of Reconstructive Surgery for Sexually Mutilated Women at the University Hospitals of Strasbourg
NCT ID: NCT06183463
Last Updated: 2023-12-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
29 participants
OBSERVATIONAL
2022-11-24
2023-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Every year, 3 million girls and young women are sexually mutilated around the world, or one woman every 15 seconds.
In recent years, a surgical repair technique has been created by a French urologist, Professor Foldès. This technique allows clitoral reconstruction. Sensory reacquisition after this intervention may take a few months, but the functional results are quite good.
There is little or no data concerning the use of reconstructive surgery for these mutilated patients consulting in sexology and the future of patients post-operatively or who have not had recourse to reconstructive surgery. The investigators then questioned the decision of these patients and their future.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
RETROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* having consulted sexology at the HUS for sexual mutilation between 01/01/2011 and 12/31/2021.
* having had clitoral repair surgery at the HUS between 01/01/2011 and 12/31/2021
* not objecting, after information, to the reuse of their data for the purposes of this research
Exclusion Criteria
* impossibility of providing the subject with informed information (difficulties in understanding the subject, etc.)
* Woman under judicial protection or under guardianship or curatorship.
18 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Strasbourg, France
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Service d'Assistance Médicale à la Procréation - CHU de Strasbourg - France
Strasbourg, , France
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Jeanine OHL, MD
Role: primary
Virginie TEISSEYRE, MD
Role: backup
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
8724
Identifier Type: -
Identifier Source: org_study_id