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NCT06811714

Comparison of Oxidants and Antioxidants in Breastmilk Under Different Anesthesia Protocols

Completed Last updated 25 November 2025
What this trial tests

trial in Oxidative Stress in 140 participants. Completed in 1 July 2025.

Timeline
6 February 2025
Primary endpoint
1 July 2025
1 July 2025

Quick facts

Lead sponsorDuzce University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment140
Start date6 February 2025
Primary completion1 July 2025
Estimated completion1 July 2025
Sites1 location across Turkey (Türkiye)

Conditions studied

Sponsor

Duzce University

Who can join

Adults 18 to 65, female only, with Oxidative Stress. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Oxidative Stress

Currently open trials in the same condition.

Other Duzce University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06811714.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing