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Clinical Trial Summary

This will be a placebo controlled, randomized, double-blind, comparative effectiveness study, in which we patients are enrolled during an emergency department (ED) visit for acute radicular low back pain (LBP) and followed by telephone two and seven days later. Patients will be randomized to receive an oral dose of dexamethasone for 2 consecutive days or placebo during an ED visit for acute radicular LBP. Every patient will receive a 7 day supply of ibuprofen and a low back pain education session.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05721027
Study type Interventional
Source Montefiore Medical Center
Contact Eddie Irizarry, MD
Phone 718-920-6626
Email eddiriza@montefiore.org
Status Recruiting
Phase Phase 4
Start date July 5, 2023
Completion date August 2025

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