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
| Type | Name | Description |
|---|---|---|
| DRUG | Acetaminophen | 1g acetaminophen is administered during skin closure (end of operation). |
| DRUG | Acetaminophen/Ibuprofen | A mixture of 1g acetaminophen and 300 mg ibuprofen (Maxigesic®IV) is administered during skin closure (end of operation) |
| DRUG | Acetaminophen | 1g acetaminophen is administered 6 hours after the first administration. |
| DRUG | Acetaminophen/Ibuprofen | A 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.