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Clitoral Reconstruction (CR) in FGM/C Patients

NCT05026814 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2023-10-18

No results posted yet for this study

Summary

Surgical interventions to reconstruct the vulva together with psychosexual care have been proposed as a multidisciplinary care concept for women who have undergone female genital mutilation/cutting (FGM/C).

This cross-sectional study is to assess the experiences of multidisciplinary care of women who request CR at Geneva University Hospital (HUG) in order to analyze the expectations and motivations for clitoral reconstruction, to study the reasons for deciding against or in favor of CR and to study the outcome of the care received (CR+ psychosexual care versus psychosexual care alone) in sexual response, eventual dyspareunia, genital self-image and overall satisfaction through questionnaires.

Conditions

  • Female Genital Mutilation / Cutting (FGM/C)

Interventions

OTHER

Interview after one year or more from the treatment received

Questionnaires to evaluate the satisfaction with treatment, the motivations and expectations for the treatment, the general well-being, the sexual function and the genital selfimage

Sponsors & Collaborators

  • University Hospital, Basel, Switzerland

    lead OTHER

Principal Investigators

  • Jasmine Abdulcadir, PD Dr. med. · Department of Obstetrics and Gynecology, University Hospital of Geneva (HUG)

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-11-19
Primary Completion
2022-02-15
Completion
2022-02-15

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05026814 on ClinicalTrials.gov