NCT04776902

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
180

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2020

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2020

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

February 25, 2021

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 2, 2021

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2021

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2021

Completed
Last Updated

June 13, 2022

Status Verified

June 1, 2022

Enrollment Period

7 months

First QC Date

February 25, 2021

Last Update Submit

June 10, 2022

Conditions

Sex BehaviorOvarian Failure

Keywords

Ovarian ReserveSexual Satisfaction

Outcome Measures

Primary Outcomes (1)

  • Sexual Satisfaction Score

    6 months

Study Arms (1)

Study Group

OTHER

All patients will be enrolled in one arm

Behavioral: Survey

Interventions

SurveyBEHAVIORAL

Patients will fill a questionary with 8 questions.

Study Group

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Patients who admitted to the gynecology clinic for any reason
  • Patients with ovarian reserve tests
  • years

You may not qualify if:

  • Mental disorders
  • Anatomic genital malformations
  • Patient' Decline to fill the survey
  • Presence of malignancy
  • Without any sexual activity

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Uludag University ART Center

Bursa, Turkey (Türkiye)

Location

Related Publications (1)

  • Kulahci Aslan E, Aslan K, Gurluler J, Uyaniklar O, Kilik T, Turk P, Ozden O, Kasapoglu I, Uncu G. EROSS study: effect of ovarian reserve on sexual satisfaction. J Obstet Gynaecol. 2022 Oct;42(7):3055-3060. doi: 10.1080/01443615.2022.2081798. Epub 2022 Jun 6.

    PMID: 35666951DERIVED

MeSH Terms

Conditions

Sexual BehaviorOrgasm

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Model Details: Survey Study
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof. Dr.

Study Record Dates

First Submitted

February 25, 2021

First Posted

March 2, 2021

Study Start

October 1, 2020

Primary Completion

May 1, 2021

Study Completion

June 1, 2021

Last Updated

June 13, 2022

Record last verified: 2022-06

Data Sharing

IPD Sharing
Will not share

Locations

TU(1)