Trials / Completed
CompletedNCT02561494
Postoperative Analgesic Effect of Nefopam
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 78 (actual)
- Sponsor
- Seoul National University Bundang Hospital · Academic / Other
- Sex
- All
- Age
- 20 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
Nefopam will be administered to the patients undergoing laparoscopic gastrectomy under the total intravenous anesthesia (TIVA). The investigators will evaluate whether the nefopam can decrease the total amount of remifentanil administered during the operation, which will reduce the acute opioid tolerance and following consumption of fentanyl during postoperative period.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Nefopam | |
| DRUG | Saline |
Timeline
- Start date
- 2015-06-01
- Primary completion
- 2016-08-01
- Completion
- 2016-08-01
- First posted
- 2015-09-28
- Last updated
- 2016-10-28
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT02561494. Inclusion in this directory is not an endorsement.