Completed

Evaluation of Depression and Sleep Disorders in Endometriosis Patients Preoperatively and Postoperatively

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Urogenital Diseases+6

+ Genital Diseases

+ Behavior

From 18 to 50 Years
+8 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: July 2019
See protocol details

Summary

Principal SponsorKanuni Sultan Suleyman Training and Research Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: July 3, 2019

Actual date on which the first participant was enrolled.

The aim of this study was to compare the depression and sleep disturbances of operated endometriosis patients before and after the operation. The main objective here is to provide data on how patients' psychological states and sleep patterns are affected by the symptoms of endometriosis and how these effects can be corrected. In this way, it is aimed to determine whether the patients have psychological support needs and to give the planned treatment due to endometriosis in the early period. As a secondary goal, it is planned to keep the patients in follow-up with their improved sleep and psychological conditions, and to improve their adherence to treatment and quality of life.

Official TitleEvaluation of Depression and Sleep Disorders in Endometriosis Patients Preoperatively and Postoperatively
NCT04009902
Principal SponsorKanuni Sultan Suleyman Training and Research Hospital
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

50 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 18 to 50 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesGenital DiseasesBehaviorBehavioral SymptomsDepressionEndometriosisFemale Urogenital Diseases and Pregnancy ComplicationsGenital Diseases, FemaleFemale Urogenital Diseases

Criteria

2 inclusion criteria required to participate
18-49 years of age with no known psychiatric disorder and
Endometriosis patients with indications for operation
6 exclusion criteria prevent from participating
Patients receiving only medical treatment without any indication for operation,
those with a known psychiatric disease,
patients with sleep disorders due to another reason,
Patients over the age of 49, patients under the age of 18,
Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 2 locations

Suspended

Kanuni Sultan Süleyman Training and Research Hospital

Istanbul, Turkey (Türkiye)Open Kanuni Sultan Süleyman Training and Research Hospital in Google Maps
Suspended

Pınar Kadiroğulları

Istanbul, Turkey (Türkiye)
Completed2 Study Centers