Trials / Completed
CompletedNCT05871424
Transdermal Buprenorphine Patch for Laparoscopic Cholecystectomy
Transdermal Buprenorphine Patch for Postoperative Pain Control in Laparoscopic Cholecystectomy: a Prospective Randomized, Placebo-controlled, Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 66 (actual)
- Sponsor
- Gangnam Severance Hospital · Academic / Other
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
Summary
Preliminary studies of the transdermal buprenorphine patch target chronic pain patients, and the pain relief effect and safety have been proven. There are previous reports that the transdermal buprenorphine patch is effective in acute postoperative pain control. However, no clinical studies have yet been reported on its application during laparoscopic cholecystectomy. Therefore, we designed this study to see if the use of a transdermal buprenorphine patch resulted in a better pain profile.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | buprenorphine patch group | 5 mcg/h buprenorphine patch will be applied preoperatively |
| DRUG | placebo group | simple dressing tape only will be applied |
Timeline
- Start date
- 2023-06-11
- Primary completion
- 2024-02-14
- Completion
- 2024-02-14
- First posted
- 2023-05-23
- Last updated
- 2024-02-26
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT05871424. Inclusion in this directory is not an endorsement.