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

StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated June 4, 2025 (before its estimated June 25, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Trial status: Not Yet Recruiting to Recruiting Primary completion date: Jun 25, 2025 to Jun 25, 2026 · Study sites: 0 to 1 · Completion date: Aug 25, 2025 to Aug 25, 2026 · 1 morev4 Show 4 more changesShow less
    • Primary completion date: Jun 25, 2025 to Jun 25, 2026
    • Study sites: 0 to 1
    • Completion date: Aug 25, 2025 to Aug 25, 2026
    • Start date changed from estimate of Aug 25, 2024 to Oct 9, 2024
  2. Start date: Jun 25, 2024 to Aug 25, 2024v3
  3. Secondary endpoints: details revised at 1 of 15 entriesv2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT06479122
Lead Sponsor Seoul National University Hospital
Conditions Cesarean Section, Postoperative Pain
Enrollment 84 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov