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Cesarean Anesthesia Blood Gas

Recruitingn/aAges 18 Years - anyFemaleBagcilar Training and Research Hospital
NCT07861633 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This prospective observational cohort study will evaluate maternal and fetal blood gas parameters in women undergoing cesarean delivery under spinal or general anesthesia. Maternal venous blood samples will be obtained immediately before anesthesia induction, and umbilical arterial blood samples will be obtained after delivery and cord clamping. Blood gas parameters, including pH, pCO2, pO2, bicarbonate, base excess, lactate, and fetal carboxyhemoglobin levels, will be compared between the spinal and general anesthesia groups. The study will also evaluate maternal-fetal blood gas gradients, Apgar scores, neonatal intensive care requirements, and the relationship between smoking exposure and fetal carboxyhemoglobin levels.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Adult women undergoing cesarean delivery at the study center. * Patients receiving spinal or general anesthesia for cesarean delivery. Exclusion Criteria: * Patients who are not eligible for participation according to the study protocol. * Patients in whom spinal anesthesia is converted to general anesthesia because of inadequate spinal block and pain during surgery.
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What it tests

  • Anesthesia Technique
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Where

1 site
Bağcılar Training and Research Hospital
Istanbul, Turkey (Türkiye)
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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