- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04776902
Effects of Ovarian Reserve on Sexual Satisfaction (EROSS)
June 10, 2022 updated by: GÜRKAN UNCU,PROF. MD, Uludag University
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
180
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Bursa, Turkey
- Uludag University ART Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 45 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: DIAGNOSTIC
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
OTHER: Study Group
All patients will be enrolled in one arm
|
Patients will fill a questionary with 8 questions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Sexual Satisfaction Score
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
October 1, 2020
Primary Completion (ACTUAL)
May 1, 2021
Study Completion (ACTUAL)
June 1, 2021
Study Registration Dates
First Submitted
February 25, 2021
First Submitted That Met QC Criteria
February 25, 2021
First Posted (ACTUAL)
March 2, 2021
Study Record Updates
Last Update Posted (ACTUAL)
June 13, 2022
Last Update Submitted That Met QC Criteria
June 10, 2022
Last Verified
June 1, 2022
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2020-2/8
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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