Thiol Disulfide Balance and Oxidative Stress Change in Endometrial Polyp Patients

February 12, 2025 updated by: Hasan Basri Savas, Mardin Artuklu University
Changes in Thiol Disulfide Balance and Oxidative Stress Mechanisms in Patients with Endometrial Polyps

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

54

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

      • Antalya, Turkey
        • Alanya Training and Research Hospital Gynecology and Obstetrics Department

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

No

Sampling Method

Probability Sample

Study Population

A total of fifty-four participants, aged 20 to 48, took part in the study, including twenty-four women diagnosed with endometrial polyps and thirty women as the control group.

Description

Inclusion Criteria:

For participants in the control group:

• To be without endometrial polyp

For the polyp group, they were as follows:

  • Individuals experiencing menometrorrhagia
  • A body mass index (BMI) of 25 or more
  • Hypertension
  • Endometrial polyps detected via saline infusion ultrasonography

Exclusion Criteria:

  • Pregnancy
  • Diabetes mellitus
  • Pelvic mass
  • Malignancy
  • The use of Tamoxifen, hormonal contraceptives, or hormone replacement therapy.

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
endometrial polyps
Women with endometrial polyp
control group
Participants in the control group were confirmed to be free of endometrial polyps via TVUSG and saline infusion ultrasonography

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Oxidative stress markers
Time Frame: From January 2021 to January 2022
Total antioxidant status (μmol Trolox equivalent/ L)
From January 2021 to January 2022
Oxidative stress markers
Time Frame: From January 2021 to January 2022
Total oxidant status (μmol H2O2 equivalent/L)
From January 2021 to January 2022
Oxidative stress markers
Time Frame: From January 2021 to January 2022
Oxidative stress index (arbitrary unit)
From January 2021 to January 2022
Oxidative stress markers
Time Frame: From January 2021 to January 2022
Paraoxonase (U/L)
From January 2021 to January 2022
Oxidative stress markers
Time Frame: From January 2021 to January 2022
Arylesterase (Ku/l)
From January 2021 to January 2022
Oxidative stress markers
Time Frame: From January 2021 to January 2022
Total thiol (µmol / L)
From January 2021 to January 2022
Oxidative stress markers
Time Frame: From January 2021 to January 2022
Native thiol (µmol / L) / alb (g / l)
From January 2021 to January 2022
Oxidative stress markers
Time Frame: From January 2021 to January 2022
Disulfide (-S-S-) (µmol / L) / alb (g/l)
From January 2021 to January 2022
Oxidative stress markers
Time Frame: From January 2021 to January 2022
Ischemia-modified albumin (u/L)
From January 2021 to January 2022

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)

January 2, 2021

Primary Completion (Actual)

January 3, 2022

Study Completion (Actual)

January 5, 2022

Study Registration Dates

First Submitted

February 7, 2025

First Submitted That Met QC Criteria

February 12, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 12, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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