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Effects of Ovarian Reserve on Sexual Satisfaction (EROSS)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04776902
Recruitment Status : Recruiting
First Posted : March 2, 2021
Last Update Posted : March 2, 2021
Sponsor:
Information provided by (Responsible Party):
GÜRKAN UNCU,PROF. MD, Uludag University

Study Description
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Brief 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.

Condition or disease Intervention/treatment Phase
Sex Behavior Ovarian Failure Behavioral: Survey Not Applicable

Study Design
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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 400 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Intervention Model Description: Survey Study
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Effects of Ovarian Reserve on Sexual Satisfaction
Actual Study Start Date : October 1, 2020
Estimated Primary Completion Date : May 1, 2021
Estimated Study Completion Date : June 1, 2021
Arms and Interventions
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Arm Intervention/treatment
Study Group
All patients will be enrolled in one arm
 Behavioral: Survey
Patients will fill a questionary with 8 questions.


Outcome Measures
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Primary Outcome Measures :
  1. Sexual Satisfaction Score [ Time Frame: 6 months ]

Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

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
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04776902


Locations
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Turkey
Uludag University ART Center Recruiting
Bursa, Turkey
Contact: Gürkan Uncu, Prof.    02242952541    guncu@gurkanuncu.org   
Sponsors and Collaborators
Uludag University
More Information
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Responsible Party: GÜRKAN UNCU,PROF. MD, Prof. Dr., Uludag University
ClinicalTrials.gov Identifier: NCT04776902    
Other Study ID Numbers: 2020-2/8
First Posted: March 2, 2021    Key Record Dates
Last Update Posted: March 2, 2021
Last Verified: February 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by GÜRKAN UNCU,PROF. MD, Uludag University:
Ovarian Reserve
Sexual Satisfaction