Clinical Trials Directory

Trials / Completed

CompletedNCT01690663

Dose Response Study of Dexamethasone in Combination With Bupivacaine 0.25%

Dose Response Study of Dexamethasone in Combination With Bupivacaine 0.25% in Ultrasound Guided Supraclavicular Brachial Plexus Nerve Block, a Randomized, Placebo Controlled Prospective Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
89 (actual)
Sponsor
University of Pennsylvania · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

When used in conjunction with a local anesthetic, dexamethasone may prolong both the sensory and motor effects of high supraclavicular brachial plexus nerve block (SBP) in arthroscopic shoulder surgery. This study seeks to determine if there is a relationship between the duration of sensory and motor blockade in supraclavicular brachial plexus nerve blocks (SBP) when combined with increasing doses of dexamethasone.

Detailed description

The exact mechanism of dexamethasone on peripheral nerve block is unclear. The current theory is that the effect is not dose related, while only 4mg and 8mg doses were studied. Our hypothesis is that the dose differences at 1mg, 2mg, or 4mg, does not have significant effect on the duration of analgesia. Therefore, we are not considering any patients to receive suboptimal dosing of preservative free dexamethasone in this study.

Conditions

Interventions

TypeNameDescription
DRUGBupivacaine 0.25%
DRUGDexamethasone
DRUGnormal salineplacebo

Timeline

Start date
2012-09-01
Primary completion
2015-02-01
Completion
2015-02-01
First posted
2012-09-24
Last updated
2017-05-04
Results posted
2017-05-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01690663. Inclusion in this directory is not an endorsement.