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NCT04776902 Clinical Trial

Effects of Ovarian Reserve on Sexual Satisfaction

Ovarian Failure Clinical Trial

— EROSS  

Official title:
Effects of Ovarian Reserve on Sexual Satisfaction

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04776902
Other study ID # 2020-2/8
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2020
Est. completion date June 1, 2021

Study information
Verified date June 2022
Source Uludag University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a survey study. The primary aim of the study is to investigate the relationship between the ovarian reserve and sexual satisfaction. All the patients who underwent ovarian reserve assessment for any reason will fill a questionnaire about sexual satisfaction. And the survey results will be compared with patients' ovarian reserve.

Recruitment information / eligibility
Status Completed
Enrollment 180
Est. completion date June 1, 2021
Est. primary completion date May 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Patients who admitted to the gynecology clinic for any reason - Patients with ovarian reserve tests - 18-45 years Exclusion Criteria: - Mental disorders - Anatomic genital malformations - Patient' Decline to fill the survey - Presence of malignancy - Without any sexual activity

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Survey
Patients will fill a questionary with 8 questions.

Locations
Country Name City State
Turkey Uludag University ART Center Bursa

Sponsors (1)
Lead Sponsor Collaborator
Uludag University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Sexual Satisfaction Score 6 months
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