CompletedNot Applicable

Comparison of Oxidants and Antioxidants in Breastmilk Under Different Anesthesia Protocols

Turkey (Türkiye)140 participantsStarted 2025-02-06

Plain-language 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.

Who can participate

Age range18 Years – 65 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients undergoing cesarean section under general or regional anesthesia * Patients in the I and II risk groups, according to the American Society of Anesthesiologists (ASA) classification Exclusion Criteria: * Pregnant women with ASA III and above, * Pregnant women with gestational DM or hypertension, * Pregnant women with an indication for Intensive Care Unit (ICU), * Pregnant women with chronic obstructive pulmonary disease, * Pregnant women with morbid obesity, * Pregnant women with a history of liver or kidney disease, * Pregnant women with coronary artery disease or heart failure, * Pregnant women with significant anemia (Hg\<7).

What they're measuring

Total oxidant status

Timeframe: Postoperative 24 hours

Total antioxidant status

Timeframe: Postoperative 24 hours

Trial details

NCT IDNCT06811714

SponsorDuzce University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-07-01

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