RecruitingPhase 4NCT06479122

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


Sponsor

Seoul National University Hospital

Enrollment

84 participants

Start Date

Oct 9, 2024

Study Type

INTERVENTIONAL

Conditions

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

Sex: FEMALEMin Age: 19 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Acetaminophen, a drug called Acetaminophen, and others for people with cesarean section and postoperative pain. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 19 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAcetaminophen

1g acetaminophen is administered during skin closure (end of operation).

DRUGAcetaminophen/Ibuprofen

A mixture of 1g acetaminophen and 300 mg ibuprofen (Maxigesic®IV) is administered during skin closure (end of operation)

DRUGAcetaminophen

1g acetaminophen is administered 6 hours after the first administration.

DRUGAcetaminophen/Ibuprofen

A mixture of 1g acetaminophen and 300 mg ibuprofen (Maxigesic®IV) is administered 6 hours after the first administration.


Locations(1)

Seoul National University Hospital

Seoul, South Korea

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NCT06479122


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