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Clinical Trials/NCT05054946
NCT05054946CompletedNot Applicable

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

Ege University1 site in 1 country55 target enrollmentStarted: October 1, 2021Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
55
Locations
1
Primary Endpoint
Change in AMH Level
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

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

Detailed 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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

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

Arms & Interventions

Endometrioma

Active Comparator

Participants who will have endometrioma after histopathological evaluation.

Intervention: Laparoscopic cystectomy (Procedure)

Mature cystic teratoma (dermoid cyst)

Active Comparator

Participants who will have mature cystic teratoma (dermoid cyst) after histopathological evaluation.

Intervention: Laparoscopic cystectomy (Procedure)

Serous or mucinous cystadenoma

Active Comparator

Participants who will have serous or mucinous cystadenoma after histopathological evaluation.

Intervention: Laparoscopic cystectomy (Procedure)

Outcomes

Primary Outcomes

Change in AMH Level

Time Frame: 6 months

AMH levels of the participants will be investigated before the surgery and 6 months after the surgery.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sabahattin Anıl Arı

Principal Investigator

Ege University

Study Sites (1)

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