Clinical Trials Directory

Trials / Completed

CompletedNCT02864602

IV Dexamethasone for Prolongation of Peripheral Nerve Block

A Volunteer Study to Determine the Optimal Dose of IV Dexamethasone Required for Prolongation of Peripheral Nerve Block

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
18 (actual)
Sponsor
University Health Network, Toronto · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

This is a volunteer study examining the effect of different doses of IV dexamethasone on prolongation of median nerve block in the forearm.

Detailed description

18 healthy volunteers aged 18-50 will be recruited (6 patients in each dosing group). Each volunteer will receive two forearm median nerve blocks separated by a two week washout period. One block will be conducted alongside an infusion of normal saline (control). The other block will be conducted alongside a randomised dose of IV dexamethasone (2, 4 or 8mg). The order of these interventions will be random. Blocks will be assessed quantitatively with cold and sharp sensation, electrical stimulation, quantitative sensory testing (thermal tolerance) and grip strength dynamometry. Measures or sensory and motor block including onset, intensity and duration will be compared between dosing groups.

Conditions

Interventions

TypeNameDescription
DRUGIV dexamethasoneAn infusion of IV dexamethasone

Timeline

Start date
2016-11-12
Primary completion
2018-02-20
Completion
2018-02-20
First posted
2016-08-12
Last updated
2019-03-04

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02864602. Inclusion in this directory is not an endorsement.