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Comparison of Oxidants and Antioxidants in Breastmilk Under Different Anesthesia Protocols

NCT06811714 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 140

Last updated 2025-11-25

No results posted yet for this study

Summary

The goal of this observational study is to determine in women undergoing cesarean section if total oxidant status and total antioxidant status in breastmilk taken at the 6th hour postoperatively changes between general and regional anesthetic protocols.

Researchers will compare general anesthesia and regional anesthesia groups to see if total oxidant status and total antioxidant status in breastmilk taken at the 6th hour postoperatively changes.

Participants will provide 2 ml of breastmilk at the 6th postoperative hour.

Conditions

  • Oxidative Stress

Sponsors & Collaborators

  • Duzce University

    lead OTHER

Principal Investigators

  • Özlem Ersoy Karka, Ass. Prof. · Düzce University Faculty of Medicine

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-02-06
Primary Completion
2025-07-01
Completion
2025-07-01

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 NCT06811714 on ClinicalTrials.gov