Endometriosis: Sexual Dysfunction and Adaptation Strategies Among Couples

Completed

• Conditions: Endometriosis
• Interventions: Other: Questionnaires

• Registration Number: NCT01402791
• Lead Sponsor: Centre Hospitalier Universitaire de Nīmes

Brief Summary

The primary objective of this study is to evaluate the presence/absence and description of persistent sexual troubles following surgical treatment for endometriosis for women, and their partners.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-01
• Study First Submitted: 2011-07-25
• Study First Submitted QC: 2011-07-25
• Study First Posted: 2011-07-26
• Primary Completion: 2011-12
• Study Completion: 2011-12
• Status Verified: 2015-03
• Last Update Submitted: 2015-03-25
• Last Update Posted: 2015-03-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• The patient (and her partner) must have given his/her informed and signed consent
• The patient (and her partner) must be insured or beneficiary of a health insurance plan
• Couples for whom the woman has formerly undergone surgical treatment for endometriosis, and for the partner agrees to respond to questionnaires for this study

Exclusion Criteria

• The patient (or her partner) is participating in another study
• The patient (or her partner) is in an exclusion period determined by a previous study
• The patient (or her partner) is under judicial protection, under tutorship or curatorship
• The patient (or her partner) refuses to sign the consent
• It is impossible to correctly inform the patient (or her partner)
• The patient is pregnant
• The patient is breastfeeding
• The patient was surgically treated for endometriosis, but was single.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
The study population	Questionnaires	All patients included according to state inclusion and exclusion criteria.

Primary Outcome Measures

Name	Time	Method
Score for the IIEF questionnaire	Day 1	Score for the IIEF questionnaire; varies from 0 to 75.
Score for the SFQ questionnaire	Day 1	Score for the SFQ questionnaire; varies from 0 to 5.

Secondary Outcome Measures

Name	Time	Method
Scores for each sub-domain of the SFQ questionnaire	Day 1	Scores for each sub-domain of the SFQ questionnaire; varies from 0 to 5.
Scores for each sub-domain of the IIEF questionnaire	Day 1	Scores for each sub-domain of the IIEF questionnaire; varies from 0 to 30.
Sexual treatment request (yes/no)	Day 1	Did the patients request treatment/help for sexual problems? yes/no

Trial Locations

Locations (1)

Centre Hospitalier Universitaire de Nîmes; 🇫🇷 Nîmes Cedex 09, Gard, France