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NCT02484196 Clinical Trial

Dyspareunia in Women With Endometriosis: Impact of Surgery on Sexual Health

Endometriosis Clinical Trial

Official title:
Dyspareunia in Women With Endometriosis: Impact of Surgery on Sexual Health

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT02484196
Other study ID # ENDODISP14
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 1, 2021
Est. completion date December 2021

Study information
Verified date January 2021
Source University of Cagliari
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Endometriosis is a disease that affects different areas of individual functioning, including the area of sexual life. Women with endometriosis have an impairment of desire and sexual arousal, orgasmic capacity reducted because of the pain and deep dyspareunia. The aim of the study is to evaluate the effectiveness of surgery on dyspareunia in women with endometriosis, taking into account other variables involved in determining dyspareunia: the quality of the couple relationship, anxiety and depression, body image, coping strategies and resilience.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 100
Est. completion date December 2021
Est. primary completion date September 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Women affected by endometriosis with dyspareunia; - Women in waiting list for surgery Exclusion Criteria: - Severe underlying comorbidities (gynecological, cardiovascular, respiratory, renal, hematological, endocrine, hepatic, gastrointestinal, neurological) - Psychiatric diseases - Refusal or inability to sign the informed consent - Pregnancy - Previous gynecological surgery - End of couple relationship

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Questionnaires
Questionnaires

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University of Cagliari

Outcome
Type Measure Description Time frame Safety issue
Primary Quality of sexual life Cases were administered and fulfilled the questionnaires at the moment of diagnosis of endometriosis up to 4weeks; Change from baseline were evalueted 2 months after surgery
See also
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