Status:
COMPLETED
Endometriosis: Sexual Dysfunction and Adaptation Strategies Among Couples
Lead Sponsor:
Centre Hospitalier Universitaire de Nīmes
Conditions:
Endometriosis
Eligibility:
All Genders
18+ years
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.
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
January 1 2011
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 1 2011
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT01402791
Start Date
January 1 2011
End Date
December 1 2011
Last Update
March 26 2015
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Centre Hospitalier Universitaire de Nîmes
Nîmes, Gard, France, 30029