- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05728281
Impact of Time on Sexual Function (FSFI® Score) After Hysterectomy (ISHYS)
July 18, 2025 updated by: University Hospital, Angers
Recommended Time to Resume Sexual Activity After Hysterectomy: Impact on Sexual Function (FSFI® Score) and Complication Rate ISHYS 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 administrative decision, psychiatric care, patient with legal protection, patient incapable of giving consent.
If our conclusions confirmed our hypothesis, it can improve clinical practices by providing additional informations for surgeon and patient, to undergo this surgery as serenely as possible.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
142
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Angers, France
- Recruiting
- University hospital of Angers
-
Contact:
- Pierre-Emmanuel BOUET, MD, PhD
- Phone Number: +33241354213
- Email: pierreemmanuel.bouet@chu-angers.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Patient ≥ 18 years old,
- Francophone,
- Sexually active,
- Receiving a conservative or non-conservative total hysterectomy for benign pathology*,
Having signed a consent form. All surgical approaches are considered, laparoscopic approach with laparoscopic or vaginal closure, vaginal approach and laparotomy.
*The indications for the procedure selected for this study include:
- Menometrorrhagia,
- Fibroids,
- Adenomyosis,
- Endometriosis,
- Pelvic statics disorder,
- Cervical dysplasia,
- Endometrial cancer not requiring lymph node dissection or additional treatment.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Resumption of sexual intercourse recommended 4 weeks after hysterectomy
|
Currently there is no consensus on the optimal time to resume sexual activity.
Using a randomization, we will therefore compare two groups: one, whose postoperative instructions will indicate a resumption of sexual activity from 4 weeks after the operation and the other from 8 weeks postoperatively.
The primary endpoint is the FSFI® score.
The patients will answer the FSFI® questionnaire preoperatively and then at 3 months after surgery.
|
|
Other: Resumption of sexual intercourse recommended 8 weeks after hysterectomy
|
Currently there is no consensus on the optimal time to resume sexual activity.
Using a randomization, we will therefore compare two groups: one, whose postoperative instructions will indicate a resumption of sexual activity from 4 weeks after the operation and the other from 8 weeks postoperatively.
The primary endpoint is the FSFI® score.
The patients will answer the FSFI® questionnaire preoperatively and then at 3 months after surgery.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Female Sexual Function Index score
Time Frame: one year
|
Assessment of the impact of the recommended time between hysterectomy and resumption of sexual intercourse on sexual function using the Female Sexual Function Index score
|
one year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postoperative complications
Time Frame: one year
|
Describe and compare postoperative complications according to the recommended time between hysterectomy and resumption of sexual intercourse.
The postoperative complications studied include dyspareunia, spontaneous pain outside of sexual intercourse, metrorrhagia, infection, and vaginal fundal suture release.
|
one year
|
|
Follow-up to the recommendation
Time Frame: one year
|
Describe the follow-up to the recommendation in terms of time to resume sexual intercourse and describe the reasons for not following the recommendation
|
one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 5, 2023
Primary Completion (Estimated)
June 5, 2026
Study Completion (Estimated)
October 5, 2026
Study Registration Dates
First Submitted
February 4, 2023
First Submitted That Met QC Criteria
February 4, 2023
First Posted (Actual)
February 15, 2023
Study Record Updates
Last Update Posted (Actual)
July 23, 2025
Last Update Submitted That Met QC Criteria
July 18, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 2022-A02714-39
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Sexual Function
-
Cairo UniversityUnknownSexual Function Disturbances | Urinary Function DisordersEgypt
-
Okan UniversityCompletedPregnancy | Female Sexual Function | Female Sexual Function During PregnancyTurkey (Türkiye)
-
Radicle ScienceCompletedSexual Function | Sexual SatisfactionUnited States
-
Rong WangCompleted
-
Assiut UniversityCompleted
-
Kanuni Sultan Suleyman Training and Research HospitalCompleted
-
Radicle ScienceCompletedSexual Function | Sexual SatisfactionUnited States
-
Suleyman Demirel UniversityCompletedMarital Relationship | Sexual Function | PostmenopauseTurkey
-
Scale Media IncCitruslabsCompletedSexual Function | Testosterone | Cognitive FunctionsUnited States
-
Genta IncorporatedCompletedNormal Renal Function | Mildly Impaired Renal Function | Moderately Impaired Renal FunctionUnited States
Clinical Trials on Recommended time after hysterectomy
-
Translational Drug DevelopmentSide-Out FoundationCompletedMetastatic Breast CancerUnited States
-
Aesculap AGB.Braun Surgical SARecruitingCervical Cancer | Endometriosis | Ovarian Cancer | Fallopian Tube Cancer | Endometrial Cancer | Uterine Prolapse | Uterine Cancer | Abnormal Uterine BleedingGermany, Spain
-
Temple UniversityUniversity of Pennsylvania; National Institute on Deafness and Other Communication...Enrolling by invitation
-
Helsinki University Central HospitalUnknown
-
University of RegensburgCompleted
-
Kaiser PermanenteMassachusetts General HospitalUnknownProlapse of Vaginal Vault After HysterectomyUnited States
-
Escola Superior de Tecnologia da Saúde do PortoCompleted
-
KU LeuvenUnknown
-
Mackay Medical CollegeRecruitingPelvic Organ Prolapse | Stage III and IV High Grade Pelvic Organ ProlapseTaiwan
-
German Center for Music Therapy ResearchHeidelberg University; Clinic of Diagnostic and Interventional Neuroradiology...Unknown