Status:
COMPLETED
Bupivacaine for Post-operative Pain in Mohs
Lead Sponsor:
University of Missouri-Columbia
Collaborating Sponsors:
University of Pennsylvania
Columbia University
Conditions:
Pain, Postoperative
Narcotic Use
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
Mohs micrographic surgery (MMS) is regarded as the gold standard for the treatment of high-risk nonmelanoma skin cancer (NMSC). Pain after MMS peaks on the day of surgery and slowly decreases thereaft...
Detailed Description
Mohs micrographic surgery (MMS) is the first-line treatment for high-risk nonmelanoma skin cancer (NMSC) and is increasingly used for melanoma and other cutaneous neoplasms. The surgical technique inv...
Eligibility Criteria
Inclusion
- a. Adult (18 years or older) patients being treated with Mohs micrographic surgery will be included in this study.
- b. Surgical procedure must include one of the following:
- Scalp rotation/transposition/advancement flap
- Ear rotation/transposition/advancement/interpolation flap or wedge repair
- Nose rotation/transposition/advancement/interpolation flap, cartilage alar-batten graft (ear donor site)
- Cheek Mustarde flap
- Lip rotation/transposition/advancement flap, wedge repair, Abbe flap
Exclusion
- c. Patients must not
- be pregnant or breastfeeding
- be taking scheduled narcotic medications
- use narcotics as a drug of abuse
- have an allergy to bupivacaine or other amide anesthetics
- have a contraindication to tramadol
- have been given narcotic pain medications during the Mohs procedure or subsequent reconstruction
- have multiple surgical sites treated on the same day
Key Trial Info
Start Date :
July 30 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 30 2021
Estimated Enrollment :
174 Patients enrolled
Trial Details
Trial ID
NCT04362566
Start Date
July 30 2020
End Date
September 30 2021
Last Update
October 21 2021
Active Locations (1)
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1
University of Missouri-Columbia
Columbia, Missouri, United States, 65212