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Endometriosis: Sexual Dysfunction and Adaptation Strategies Among Couples (DYSEXTRIOSE)

C

Centre Hospitalier Universitaire de Nīmes

Status

Completed

Conditions

Endometriosis

Treatments

Other: Questionnaires

Study type

Observational

Funder types

Other

Identifiers

NCT01402791
LOCAL/2011/SD-05
2011-A00564-37 (Other Identifier)

Details and patient eligibility

About

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.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

60 participants in 1 patient group

The study population
Description:
All patients included according to state inclusion and exclusion criteria.
Treatment:
Other: Questionnaires

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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