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Clinical Trial Summary

This study will look at the efficacy of dexamethasone for prolongation of peripheral nerve blocks.


Clinical Trial Description

The purpose of this randomized, double-blinded, placebo-controlled trial is to examine if dexamethasone given perineurally as an adjuvant to the nerve block will prolong the time to recovery from sensory nerve block from a saphenous (or adductor canal) nerve block. The primary outcome will be time to resolution of the nerve block as assessed by pinprick over the saphenous nerve distribution. If this primary end point is met, this study will also serve as an equivalency dosing study comparing 1 mg of perineural dexamethasone to 4 mg of perineural dexamethasone. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02462148
Study type Interventional
Source Wake Forest University Health Sciences
Contact
Status Completed
Phase Phase 4
Start date July 2015
Completion date August 31, 2017

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