Clinical Trials Directory

Trials / Completed

CompletedNCT03797924

Intercostobrachial Nerve Block (ICBN) for Tourniquet Pain: Is it Necessary?

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
46 (actual)
Sponsor
University of Florida · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

In this study the investigators would like to show that when patients undergo upper limb surgery under supraclavicular brachial plexus block, additional blocking of the Intercostobrachial Nerve Block (ICBN) does not affect the incidence or course of tourniquet pain.

Detailed description

The ICBN is a cutaneous sensory nerve that supplies the medial aspect of the upper arm. Traditionally this nerve is blocked to alleviate tourniquet pain. The etiology of tourniquet pain is complex and the study team hypothesize that blocking the ICBN has no impact on tourniquet pain. Patients will receive a supraclavicular block and be divided into two groups; ICBN with local anesthetic or ICBN with saline. All patients in this study will receive a supraclavicular block as their primary anesthetic and then be divided into two groups; those who receive ICBN and those who do not. Amount of intraoperative analgesics, conversion to deep sedation or general anesthesia, and onset of time to tourniquet pain will be the primary measures of this study.

Conditions

Interventions

TypeNameDescription
DRUGReceive ICBN with ropivacaineICBN block will be performed using US guidance depositing 10 ml of 0.5% ropivacaine in the plane between pectoralis minor and serratus anterior over the 2nd and 3rd intercostal space.
BEHAVIORALNo ICBN blockThe site of injection will be prepped with tinted chlorhexidine

Timeline

Start date
2019-04-25
Primary completion
2020-12-20
Completion
2021-12-13
First posted
2019-01-09
Last updated
2022-05-24

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03797924. Inclusion in this directory is not an endorsement.