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Clinical Trials/NCT04009902
NCT04009902
Completed
Not Applicable

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

Kanuni Sultan Suleyman Training and Research Hospital2 sites in 1 country50 target enrollmentJuly 3, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endometriosis
Sponsor
Kanuni Sultan Suleyman Training and Research Hospital
Enrollment
50
Locations
2
Primary Endpoint
Beck Depression Scale
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
July 3, 2019
End Date
May 3, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pınar Kadirogulları

Principal investigator, M.D, Department of Obstetrics and Gynecology

Kanuni Sultan Suleyman Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • 18-49 years of age with no known psychiatric disorder and
  • Endometriosis patients with indications for operation

Exclusion Criteria

  • 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,
  • Patients with malignancy,
  • pregnant women

Outcomes

Primary Outcomes

Beck Depression Scale

Time Frame: 1 week

postoperative depression in endometriosis patients will be evaluated. Consists of 21 questions scored between 0-3. HIGH SCORE SHOWS TO HIGH DEPRESSION. (0-63 POINTS)

Pittsburgh Sleep Quality Index

Time Frame: 1 week

postoperative sleep disorders of endometriosis patients will be evaluated. Consists of 9 questions scored between 0-3. HIGH SCORE SHOWS BAD SLEEP QUALITY. (0-27 POINTS)

Study Sites (2)

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