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Trials / Recruiting

RecruitingNCT06479122

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

Efficacy of Intravenous Acetaminophen Alone Versus Combination of Acetaminophen/Ibuprofen (Maxigesic®IV) in Multimodal Analgesia After Cesarean Section: a Randomized Controlled Trial

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
84 (estimated)
Sponsor
Seoul National University Hospital · Academic / Other
Sex
Female
Age
19 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGAcetaminophen1g acetaminophen is administered during skin closure (end of operation).
DRUGAcetaminophen/IbuprofenA mixture of 1g acetaminophen and 300 mg ibuprofen (Maxigesic®IV) is administered during skin closure (end of operation)
DRUGAcetaminophen1g acetaminophen is administered 6 hours after the first administration.
DRUGAcetaminophen/IbuprofenA mixture of 1g acetaminophen and 300 mg ibuprofen (Maxigesic®IV) is administered 6 hours after the first administration.

Timeline

Start date
2024-10-09
Primary completion
2026-06-25
Completion
2026-08-25
First posted
2024-06-28
Last updated
2025-06-04

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06479122. Inclusion in this directory is not an endorsement.