Clinical Trials Directory

Trials / Completed

CompletedNCT00674622

Prolotherapy for the Treatment of Chronic Lateral Epicondylitis

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
67 (actual)
Sponsor
University of Pittsburgh · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Lateral epicondylitis (LE), or tennis elbow, is a common and often disabling condition affecting young and middle-aged adults-most commonly manual workers and recreational athletes. It results in significant pain and disability, limiting work productivity and an individual's ability to participate in and enjoy recreational activities. Like many other chronic musculoskeletal conditions LE often shows an incomplete response to acute treatments, leading to chronic pain and disability. Prolotherapy (PrT) involves the injection of an irritant or proliferant solution into tendons, ligaments, and joints to treat chronic musculoskeletal pain. We will be conducting a 3-group randomized, blinded trial to determine the safety and efficacy of PrT injections in the treatment of chronic LE. Additionally, we will seek to determine to what extent any beneficial effect of PrT is derived from deep needle placement vs. a specific effect of the injectate. The specific aims for this study are: 1) to determine if PrT is a safe, well-tolerated, and effective treatment for individuals with chronic LE; and 2) to determine whether the deep needle placement alone is responsible for the therapeutic effect, independent of injectate. In order to accomplish these aims, we will measure indicators of pain and disability using self-rating scales, questionnaires and physical measures. Subjects will be stratified prior to randomization on two factors: 1) unilateral vs. bilateral LE; and 2) treatment with steroids within the prior 6 months. If effective, subjects receiving PrT will show greater reduction of pain and functional impairment compared with the other two groups. This research will guide future studies on prolotherapy by determining what may be the best control condition. Additionally, further studies may explore the mechanism responsible for any beneficial effect.

Detailed description

Same

Conditions

Interventions

TypeNameDescription
DRUGProlotherapyInjection of 15% dextrose with lidocaine at the lateral epicondyle
PROCEDUREPlaceboSaline/lidocaine

Timeline

Start date
2007-09-01
Primary completion
2010-10-01
Completion
2011-10-01
First posted
2008-05-08
Last updated
2016-05-16
Results posted
2016-05-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00674622. Inclusion in this directory is not an endorsement.