N/A
N=10
The Effect of Intravenous Lidocaine on Allodynia
Pain
Bottom Line
View on ClinicalTrials.gov: NCT00659633 ↗Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Jun 2017
Primary outcome: Primary: Pain Perception — 5.40303; 5.1457; 5.13171 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- lidocaine (Drug)
- Age
- Adult, Older Adult · 19+ yrs
- Sex
- All
- Sponsor
- University of Alabama at Birmingham
- Primary completion
- Jun 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pain Perception |
5.40303; 5.1457; 5.13171 | — |
Summary
The purpose of this study is to study if lidocaine, given intravenously, reduces pain.
Eligibility Criteria
Inclusion Criteria
- Chronic Regional Pain Syndrome diagnostic criteria by the Work Safe BC. vi
Exclusion Criteria
- History of Substance abuse
- Other Medications: CRPS patients are expected to be treated for chronic pain, whether the current treatment regimen interferes with sensory motor testing will be determined on a case by case basis.
- Coronary Artery Disease (CAD): unstable
- Congestive Heart Failure (CHF): unstable
- Heart Arrhythmia: symptomatic
- Chronic Obstructive Pulmonary Disease (COPD)
- Lidocaine Allergy
- Diagnostic and Statistical Manual of Mental Disorders (Rev IV): Axis I: Common Axis I disorders include depression, anxiety disorders, bipolar disorder, ADHD, and schizophrenia. Axis II: borderline personality disorder, schizotypal personality disorder, antisocial personality disorder, and mild mental retardation.
- Presence of Contraindications for MRI
- Presence of electronically, magnetically, and mechanically activated implants
- Electronically, magnetically, and mechanically activated implants
- Ferromagnetic or electronically operated active devices like automatic cardioverter defibrillators
- Cardiac pacemakers
- Metallic splinters in the eye
- Ferromagnetic haemostatic clips in the central nervous system (CNS)
- Claustrophobia
- Pregnancy
Data sourced from ClinicalTrials.gov (NCT00659633). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.