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Endometriosis: Sexual Dysfunction and Adaptation Strategies Among Couples

Endometriosis: Sexual Dysfunction and Adaptation Strategies Among Couples

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01402791
Acronym
DYSEXTRIOSE
Enrollment
60
Registered
2011-07-26
Start date
2011-01-31
Completion date
2011-12-31
Last updated
2015-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis

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.

Interventions

OTHERQuestionnaires

All included couples (women and their partners) are required to fill out several questionnaires: 1. Questionnaire for women; 2. Self-questionnaire for women; 3. SFQ for women; 4. Questionnaire for men; 5. Self-questionnaire for men; 6. IIEF for men.

Sponsors

Centre Hospitalier Universitaire de Nīmes
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Score for the SFQ questionnaireDay 1Score for the SFQ questionnaire; varies from 0 to 5.
Score for the IIEF questionnaireDay 1Score for the IIEF questionnaire; varies from 0 to 75.

Secondary

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

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026