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Completed

NCT Number: NCT01402791

Endometriosis: Sexual Dysfunction and Adaptation Strategies Among Couples

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.

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Key information

Conditions

Endometriosis Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Genital Diseases Genital Diseases, Female Urogenital Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Centre Hospitalier Universitaire de Nîmes

Nîmes, Gard, 30029, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

questionnaires

Other

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.

Primary outcomes

  1. Score for the SFQ questionnaire

    Time frame: Day 1

    Score for the SFQ questionnaire; varies from 0 to 5.

  2. Score for the IIEF questionnaire

    Time frame: Day 1

    Score for the IIEF questionnaire; varies from 0 to 75.

Secondary outcomes

  1. Scores for each sub-domain of the SFQ questionnaire

    Time frame: Day 1

    Scores for each sub-domain of the SFQ questionnaire; varies from 0 to 5.

  2. Scores for each sub-domain of the IIEF questionnaire

    Time frame: Day 1

    Scores for each sub-domain of the IIEF questionnaire; varies from 0 to 30.

  3. Sexual treatment request (yes/no)

    Time frame: Day 1

    Did the patients request treatment/help for sexual problems? yes/no

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Nīmes

Other

Registry information

Acronym: DYSEXTRIOSE

Important dates

Study start
2011
Primary completion
2011
Study completion
2011
First posted
Jul 26, 2011
Registry last updated
Mar 26, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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