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Evaluation of Thioldisulfide Balance in Cervical Preinvasive Lesions

NCT04177641 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2020-02-06

No results posted yet for this study

Summary

The purpose of this study is to investigate Thiol-disulfide balance in patients with cervical preinvasive lesions

Conditions

  • Oxidative Stress
  • Low Grade Squamous Intraepithelial Lesion
  • High-Grade Squamous Intraepithelial Lesions

Interventions

DIAGNOSTIC_TEST

Disulphide(μmol/L)

Aforementioned oxidative stress markers will be measured via Cobas c501(Roche Diagnostics, Indianapolis, IN, USA) used with sphectrophotometry

DIAGNOSTIC_TEST

Total Oxidant Capacity(μmolH2O2Equiv/L)

Aforementioned oxidative stress markers will be measured via Cobas c501(Roche Diagnostics, Indianapolis, IN, USA) used with sphectrophotometry

Sponsors & Collaborators

  • Muğla Sıtkı Koçman University

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-09-20
Primary Completion
2020-01-01
Completion
2020-01-10

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04177641 on ClinicalTrials.gov