Viewing Study NCT02060734


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Study NCT ID: NCT02060734
Status: WITHDRAWN
Last Update Posted: 2017-02-23
First Post: 2014-02-07
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Lidocaine Injection Versus Sham Needling in Treating Whiplash Associated Disorder
Sponsor: Hamilton Health Sciences Corporation
Organization:

Study Overview

Official Title: Lidocaine Injection Versus Sham Needling in Treating Whiplash Associated disorder-a Randomized Controlled Trial
Status: WITHDRAWN
Status Verified Date: 2015-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: no participant recruited
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To determine the efficacy of lidocaine injection of trigger points versus subcutaneous injection in patients with subacute whiplash associated disorder following injury.
Detailed Description: This is a double-blind, randomized controlled trial to determine the efficacy of lidocaine injection of trigger points versus subcutaneous injection in patients with subacute whiplash associated disorder following injury. Outcomes include pain, objective assessment, self-report function recovery, impact on work performance and globe perceived effects which will be assessed 5 minutes, 2 and 6 weeks following injection.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: