Trials / Completed
CompletedNCT03644147
Additive Effect of Intravenous Acetaminophen on Postoperative Pain Control
Additive Effect of Intravenous Acetaminophen Administered at the End of Surgery on Postoperative Pain Control With Nefopam and Fentanyl-based Patient-controlled Analgesia: A Double-blind Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 84 (actual)
- Sponsor
- Seoul National University Hospital · Academic / Other
- Sex
- Female
- Age
- 19 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This study aimed to evaluate the additive effect of acetaminophen on postoperative pain control in patients receiving nefopam and fentanyl-based patient-controlled analgesia. Participants undergoing laparoscopic hysterectomy will be randomly assigned to treatment group or control group. After end of surgery, acetaminophen or normal saline (placebo) will be administered intravenously depending on the group assigned.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Acetaminophen | Acetaminophen will be intravenously administrated to treatment group after the end of surgery. |
Timeline
- Start date
- 2018-08-27
- Primary completion
- 2021-01-06
- Completion
- 2021-01-07
- First posted
- 2018-08-23
- Last updated
- 2021-01-08
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03644147. Inclusion in this directory is not an endorsement.