Endometriosis: Sexual Dysfunction and Adaptation Strategies Among Couples

NCT ID: NCT01402791

Last Updated: 2015-03-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-01-31

Study Completion Date

2011-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Endometriosis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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The study population

All patients included according to state inclusion and exclusion criteria.

Questionnaires

Intervention Type 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.

Interventions

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Questionnaires

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.

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Nīmes

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Stéphane Droupy, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universitaire de Nîmes

Locations

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Centre Hospitalier Universitaire de Nîmes

Nîmes, Gard, France

Site Status

Countries

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France

Other Identifiers

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2011-A00564-37

Identifier Type: OTHER

Identifier Source: secondary_id

LOCAL/2011/SD-05

Identifier Type: -

Identifier Source: org_study_id

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