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Recruiting Phase 4 NCT06479122

Efficacy of Acetaminophen Alone Versus Combination of Acetaminophen/Ibuprofen After Cesarean Section

Trial Parameters

Condition Cesarean Section
Sponsor Seoul National University Hospital
Study Type INTERVENTIONAL
Phase Phase 4
Enrollment 84
Sex FEMALE
Min Age 19 Years
Max Age N/A
Start Date 2024-10-09
Completion 2026-06-25
Interventions
AcetaminophenAcetaminophen/IbuprofenAcetaminophen

Brief Summary

The investigators aim to compare the analgesic efficacy of intravenous acetaminophen alone versus combination of acetaminophen/ibuprofen (Maxigesic®IV) in multimodal analgesia after cesarean section.

Eligibility Criteria

Inclusion Criteria: * Patients scheduled for elective cesarean section * Gestational age \> 37+0 weeks Exclusion Criteria: * Emergency cesarean section * Multiple pregnancy (e.g. twins, triplets) * Body weight \< 50 kg * Preeclampsia * History of hypersensitivity to acetaminophen or ibuprofen * History of upper gastrointestinal tract bleeding or gastric ulcer * Underlying liver disease * Underlying kidney disease or GFR \< 90 mL/min/1.73m2 * Heart failure or severe hypertension * History of asthma * Chronic use of barbital or tricyclic antidepressants

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