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Study identifier: NCT05728281 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Impact of Time on Sexual Function (FSFI® Score) After Hysterectomy

Condition: Time Between Hysterectomy and Resumption of Sexual Relations · Sexual Function  ·  Sponsor: University Hospital, Angers

PhaseNA
Planned participants142
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersYes

About this study

In France, more than 62 000 hysterectomies are performed each year. Female sexual function is the result of multiple psychological, social and physiological factors. There is no information in the current literature about the optimum time between the surgery and the sexual relation resumption. The primary outcome is to assess the impact of advising time between hysterectomy and sexual relation resumption by using FSFI® score. Secondaries outcomes are: to describe and compare post-operative complications in the two groups of the study, to describe the follow-up of the recommendation concerning time between surgery and sexual relation resumption and to describe why this recommendation was not followed. This study is based on 4 questionnaires: FSFI® pre-operative and post-operative, pre-operative questionnaire and post-operative questionnaire. This is a monocentric, comparative, of superiority, randomised and prospective study. Patients are randomised into two groups: sexual relation resumption advised 4 weeks after surgery, or 8 weeks. The inclusion criteria are more than 18 years, francophone, in sexual activity, scheduled for a total hysterectomy for benign indication (menometrorrhagia, fibroma, adenomyosis, endometriosis, pelvic floor disorders, low-grade endometrial cancer), considering vaginal, laparoscopic and abdominal approach, and a written consent. Non-inclusion criteria are illiteracy, cognitive disorders, without social security, deprived liberty by judicial or admi…

This description comes directly from the study's public registry record.

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Locations (1)

University Hospital of AngersAngers, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT05728281