NCT01583179

Duration of Analgesic Effect for Ultrasound Guided Supraclavicular Blocks With the Addition of Buprenorphine to Local Anesthetic Solution

• Status: Terminated
• Phase: N/A
• Study type: Interventional
• Enrollment: 26 (actual)
• Sponsor: University of Wisconsin, Madison · Academic / Other
• Sex: All
• Age: 18 Years – 79 Years
• Healthy volunteers: Not accepted

Summary

The patients included will be those who have already agreed to have a brachial plexus nerve block for surgery. A flip of the coin will decide who gets and additive called buprenorphine in their block or not. They will both contain the same amount and type of numbing medicine. The goal will be to see if the additive extends the life of the pain control portion of the ultrasound guided supraclavicular nerve block.

Conditions

• Regional Block for Pain Control
• Supraclavicular Block
• Ultrasound Guided Block
• Block Additive

Interventions

Type	Name	Description
DRUG	Buprenorphine	added to nerve block, 0.3mg one time peripheral block use

Timeline

• Start date: 2012-04-01
• Primary completion: 2014-03-01
• Completion: 2015-12-01
• First posted: 2012-04-23
• Last updated: 2019-09-11
• Results posted: 2019-09-11

Locations

1 site across 1 country: United States