- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06826495
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
Conditions
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
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Antalya, Turkey
- Alanya Training and Research Hospital Gynecology and Obstetrics Department
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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
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 |
|---|
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endometrial polyps
Women with endometrial polyp
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control group
Participants in the control group were confirmed to be free of endometrial polyps via TVUSG and saline infusion ultrasonography
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Oxidative stress markers
Time Frame: From January 2021 to January 2022
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Total antioxidant status (μmol Trolox equivalent/ L)
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From January 2021 to January 2022
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Oxidative stress markers
Time Frame: From January 2021 to January 2022
|
Total oxidant status (μmol H2O2 equivalent/L)
|
From January 2021 to January 2022
|
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Oxidative stress markers
Time Frame: From January 2021 to January 2022
|
Oxidative stress index (arbitrary unit)
|
From January 2021 to January 2022
|
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Oxidative stress markers
Time Frame: From January 2021 to January 2022
|
Paraoxonase (U/L)
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From January 2021 to January 2022
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Oxidative stress markers
Time Frame: From January 2021 to January 2022
|
Arylesterase (Ku/l)
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From January 2021 to January 2022
|
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Oxidative stress markers
Time Frame: From January 2021 to January 2022
|
Total thiol (µmol / L)
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From January 2021 to January 2022
|
|
Oxidative stress markers
Time Frame: From January 2021 to January 2022
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Native thiol (µmol / L) / alb (g / l)
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From January 2021 to January 2022
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Oxidative stress markers
Time Frame: From January 2021 to January 2022
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Disulfide (-S-S-) (µmol / L) / alb (g/l)
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From January 2021 to January 2022
|
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Oxidative stress markers
Time Frame: From January 2021 to January 2022
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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.
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)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 10354421-2020/23-8
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.