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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

TypeNameDescription
DRUGbuprenorphine patch group5 mcg/h buprenorphine patch will be applied preoperatively
DRUGplacebo groupsimple 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.

Transdermal Buprenorphine Patch for Laparoscopic Cholecystectomy (NCT05871424) · Clinical Trials Directory