Endometriosis: Sexual Dysfunction and Adaptation Strategies Among Couples

Centre Hospitalier Universitaire de Nīmes1 site in 1 country60 target enrollmentJanuary 2011

ConditionsEndometriosis

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Endometriosis
Sponsor: Centre Hospitalier Universitaire de Nīmes
Enrollment: 60
Locations: 1
Primary Endpoint: Score for the IIEF questionnaire
Status: Completed
Last Updated: 11 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

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.

Registry

clinicaltrials.gov

Start Date

January 2011

End Date

December 2011

Last Updated

11 years ago

Study Type

Observational

Sex

All

Investigators

Sponsor

Centre Hospitalier Universitaire de Nīmes

Responsible Party

Sponsor

Eligibility Criteria

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.