MedTrace Logo

Oral Dexamethasone for the Treatment of Cervical Radiculopathy

NCT00308594 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2011-04-28

No results posted yet for this study

Summary

The purpose of this study is to determine whether dexamethasone is effective in the treatment of pain and disability resulting from a compressed spinal nerve in the neck (cervical radiculopathy).

Conditions

  • Cervical Radiculopathy

Interventions

DRUG

Dexamethasone

Sponsors & Collaborators

  • University of Manitoba

    lead OTHER

Principal Investigators

  • Dave R Hooper, MD BSc · University of Manitoba

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-11-30
Primary Completion
2007-11-30
Completion
2007-11-30

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00308594 on ClinicalTrials.gov