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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05527665
Other study ID # 38RC21.0301
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date September 2022
Est. completion date December 2022

Study information

Verified date September 2022
Source University Hospital, Grenoble
Contact Marie Bugnon
Phone +33684722204
Email mar.bugnon@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Evaluation of the sexual quality of life of women who had a sub-urethral sling several years ago, using a recently validated questionnaire: the PPSSQ (Pelvi-Perineal Surgery Sexuality Questionnaire). This questionnaire is specifically oriented for women who have undergone surgery for stress urinary incontinence or prolapse. It contains questions specific to post-surgical issues that are not present in other sexual quality of life questionnaires. The questionnaire will also be administered to a group of control women who have not had suburethral sling surgery in order to compare their responses to those of women who have had surgery. The hypothesis is that the placement of a suburethral sling for stress urinary incontinence increases the quality of sexual life of the women.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date December 2022
Est. primary completion date December 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: Patient group - Women who have received a suburethral sling at CHUGA in the gynecology or urology departments between January 2015 and June 2020. - Women who agreed to complete the PPSSQ Healthy volunteers group - Adult women matched on age and menopausal status to the patient group - Women who have never undergone surgery for stress urinary incontinence by placing a sub-urethral tape. - Women who agreed to complete the PPSSQ Exclusion Criteria: Patient group - Tape removal. - Death since surgery. - Factors that make it impossible to understand the questionnaires: neurological or psychiatric pathology that limits the understanding of the questions, lack of mastery of the French language, illiteracy. - Absence of perineal sensation. - Persons referred to in articles L1121-5 to L1121-8 of the CSP. Healthy volunteers group - Factors that make it impossible to understand the questionnaires: neurological or psychiatric pathology that limits the understanding of the questions, lack of mastery of the French language, illiteracy. - Absence of perineal sensation. - Persons referred to in articles L1121-5 to L1121-8 of the CSP.

Study Design


Intervention

Procedure:
Midurethral sling surgery
This treatment consists of the placement of a sub-urethral sling, usually made of polypropylene, in order to support the urethra during efforts and thus to avoid leaks linked to its hyper mobility. This is a frequent and rapid surgery, which is performed on an outpatient basis. The sling is placed under the patient's urethra with the help of an awl.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Grenoble

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluate the sexual discomfort in the medium term in patients who have undergone surgery for stress urinary incontinence by placing a suburethral sling. The primary endpoint of the research is the comparison of medians of the PPSSQ "discomfort and pain" score between women who underwent suburethral sling surgery and healthy female volunteers of the same age and menopausal status. 2 to 7 years after the surgery
Secondary To evaluate the quality of sexual life of patients who have undergone surgery for stress urinary incontinence using a suburethral sling. Comparison of medians of the PPSSQ "sexual health" score between women with suburethral sling surgery and healthy female volunteers. 2 to 7 years after the surgery
Secondary Analyze the causes of discomfort and the characteristics of pain experienced by patients during intercourse. Analyse of PPSSQ answers to questions 5 and 6 2 to 7 years after the surgery
Secondary To analyze the rate of non-sexually active patients after surgery, and the causes of this lack of sexuality. Analyse of PPSSQ answers to question 1 2 to 7 years after the surgery
Secondary Compare sexual discomfort and quality of sexual life before/after suburethral sling surgery. Comparison of medians of the PPSSQ scores in the patient group before and after surgery 2 to 7 years after the surgery
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