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NCT05054946 Clinical Trial

The Effect of Laparoscopic Surgery on Ovarian Reserve According to Cyst Types

Ovarian Cysts Clinical Trial

Official title:
The Effect of Laparoscopic Surgery on Ovarian Reserve According to Cyst Types

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05054946
Other study ID # 17/056
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2021
Est. completion date September 1, 2022

Study information
Verified date September 2022
Source Ege University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of our study is to compare the effect of laparoscopic ovarian cystectomy on ovarian reserve in terms of different cyst types.

Description:

Participants who will be treated surgically for ovarian cysts will be included in the study. Anti-Mullerian Hormone (AMH) levels of the participants will be investigated before the surgery and 6 months after the surgery. All surgeries will be performed under general anesthesia laparoscopically. After histopathological evaluation, the participants will be divided into three groups; Group 1: Endometrioma, Group 2: Mature cystic teratoma (Dermoid cyst) and Group 3: Serous or mucinous cystadenoma. A total of fifty-five women will be included in the study.

Recruitment information / eligibility
Status Completed
Enrollment 55
Est. completion date September 1, 2022
Est. primary completion date September 1, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - no ovarian surgery before Exclusion Criteria: - Endocrinological pathologies - Suspicion of malignancy in preoperative laboratory and ultrasonographic evaluations - Detection of malignancy in histopathological examination

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Laparoscopic cystectomy
All surgeries will be performed under general anesthesia by laparoscopically.

Locations
Country Name City State
Turkey Ege University Hospital Izmir

Sponsors (1)
Lead Sponsor Collaborator
Ege University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in AMH Level AMH levels of the participants will be investigated before the surgery and 6 months after the surgery. 6 months
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