- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06903650
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
Status
Completed
Conditions
Intervention / Treatment
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
-
-
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İzmir, Turkey, 35000
- Dokuz Eylul University School of Medicine
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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:
- Women between the ages of 37-45 with continuing menstrual cycles (37 and 45 included)
- Patients who will undergo uterine surgery for benign reasons or who will undergo salpingectomy only due to hydrosalpinx, ectopic pregnancy, tubo-ovarian abscess
- Patients who have not had ovarian surgery before
- Those without menopause and premature ovarian failure
- Patients who accept the study
Exclusion Criteria:
- Age younger than 37 or older than 45
- Those who want to withdraw from the study
- Those who do not come for follow-up examination
- Use of drugs that affect ovarian reserve
- Any surgical procedure performed on the ovaries during the operation
- No menstrual bleeding in the last year
- 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
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|
postoperative days 2 ovarian arter pulsatility index (PI) (right and left)
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The effect of salpingectomy operation on ovarian reserve
|
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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.
Sponsor
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
Other Study ID Numbers
- SOORAMHODU
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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