The Effect of Salpingectomy Operation on Ovarian Reserve

March 31, 2025 updated by: Derya Öztürk, Dokuz Eylul University

Evaluation of the Effect of Salpingectomy Operation on Ovarian Reserve With Anti-Mullerian Hormone and Ovarian Doppler Ultrasonography

This study aimed to evaluate the effect of salpingectomy operation on ovarian reserve. Ovarian reserve was evaluated by measuring anti-mullerian hormone levels from serum samples taken from the patients before the operation and 6 weeks after the operation. Ovarian doppler flow were evaluated by measuring the ovarian artery pulsatility index with transvaginal ultrasonography preoperatively, postoperative days 2 and postoperative weeks 6 . In our study, it was determined that ovarian functions may be negatively affected in the acute period after salpingectomy operation.

Study Overview

Study Type

Observational

Enrollment (Actual)

31

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • İzmir, Turkey, 35000
        • Dokuz Eylul University School of Medicine

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Serum samples will be separated from routine blood samples taken from patients who apply to the outpatient clinic and will undergo salpingectomy within the indication, during perioperative preparation and at the 6th week postoperatively, after patient consent is obtained. This serum sample will be taken into an Eppendorf tube and kept at -40˚C for later AMH levels to be studied. Ovarian artery pulsatility index values measured during the patient's perioperative and postoperative routine ultrasonographic examination and weeks 6 postoperative control will be recorded.

Description

Inclusion Criteria:

  1. Women between the ages of 37-45 with continuing menstrual cycles (37 and 45 included)
  2. Patients who will undergo uterine surgery for benign reasons or who will undergo salpingectomy only due to hydrosalpinx, ectopic pregnancy, tubo-ovarian abscess
  3. Patients who have not had ovarian surgery before
  4. Those without menopause and premature ovarian failure
  5. Patients who accept the study

Exclusion Criteria:

  1. Age younger than 37 or older than 45
  2. Those who want to withdraw from the study
  3. Those who do not come for follow-up examination
  4. Use of drugs that affect ovarian reserve
  5. Any surgical procedure performed on the ovaries during the operation
  6. No menstrual bleeding in the last year
  7. Patients who received radiotherapy and hormonal therapy within 3 months before surgery

Study Plan

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

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
perioperative ovarian arter pulsatility index(PI)(right and left), perioperative AMH levels
The effect of salpingectomy operation on ovarian reserve
postoperative days 2 ovarian arter pulsatility index (PI) (right and left)
The effect of salpingectomy operation on ovarian reserve
postop. weeks 6 ovarian arter pulsatility index(PI)(right and left), postop. weeks 6 AMH levels
The effect of salpingectomy operation on ovarian reserve

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
right ovarian arter pı
Time Frame: perioperative, postoperative days 2 , postoperative weeks 6
rate of 0,87/ 0,84/ 0,76
perioperative, postoperative days 2 , postoperative weeks 6
left ovarian arter pı
Time Frame: perioperative, postoperative days 2, postoperative weeks 6
rate of 0,89/ 0,79/ 0.80
perioperative, postoperative days 2, postoperative weeks 6
AMH levels
Time Frame: perioperative-postoperative weeks 6
Concentration of 1 ng/mL / 0,79 ng/mL
perioperative-postoperative weeks 6

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 27, 2020

Primary Completion (Actual)

March 3, 2021

Study Completion (Actual)

June 5, 2021

Study Registration Dates

First Submitted

March 21, 2025

First Submitted That Met QC Criteria

March 28, 2025

First Posted (Actual)

March 31, 2025

Study Record Updates

Last Update Posted (Actual)

April 3, 2025

Last Update Submitted That Met QC Criteria

March 31, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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