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The effectiveness of therapeutic laser treatment for elbow tendonitis (tennis elbow)
DOI 10.1186/ISRCTN04330904
ClinicalTrials.gov identifier
EudraCT number
Public title The effectiveness of therapeutic laser treatment for elbow tendonitis (tennis elbow)
Scientific title The efficacy of therapeutic class IV laser treatment for epicondylitis: a randomized controlled trial
Acronym N/A
Serial number at source N/A
Study hypothesis We hypothesize that when administered in eight treatments over 21 days with a total dose per treatment of 3000 J (6.6 ± 1.3 J/cm2) therapeutic class IV laser therapy will be effective in a clinical setting for the long term alleviation of the pain, loss of strength and dysfunction of tendinopathy of the extensor carpi radialis brevis tendon.
Lay summary Background and study aims
Tendonitis (inflammation of a tendon) is a very common condition for which there is still no reliable treatment. One method which has shown promise is low level laser therapy (LLLT), however the findings from studies examining the ability of LLLT to lessen the pain, loss of strength and dysfunction of tendonitis are not clear. Recently, a new higher power laser instrument has been developed which is capable of delivering a dose much faster. Thus, the purpose of this investigation was to determine the effectiveness of this new instrument for the treatment of one specific type of tendonitis (tennis elbow or lateral epicondylitis).

Who can participate?
Participants were recruited by advertisement in the newspaper in Toledo Ohio in the fall of 2009. Only otherwise healthy volunteers with tennis elbow were accepted, about half of them were women and half were men. The average age was around 50 years of age, and most of them had suffered from tendonitis of the elbow for over 2 years.

What does the study involve?
Once participants had been checked by a physician to make sure that they had tendonitis of the elbow they were randomly assigned to one of two groups. Group A received the true treatment, group B received a treatment from an identical machine but instead of a laser it had a regular light. None of the doctors or patients knew which machine was which, there was no way to tell the difference between the two. Each treatment took about 10 minutes, and there were 8 treatments in total over three weeks. No one was allowed to use other types of treatments during the study.
At the end of the treatment series the participants were checked again for signs of tendonitis including pain, strength, function and an ultrasound. They came back three more times over the next year to see if their elbows still felt better. After 3 months though, the participants who were in group B were offered the chance to try the real laser. The study concluded in January of 2011.

What are the possible benefits and risks of participating?
The benefits to participating in this study were the opportunity to help find an effective treatment for elbow tendonitis and to receive this treatment free of charge.
The risks of the treatment are very low. The laser is powerful enough to damage a personís eyes, but participants were given protective goggles to wear. There were no side effects from the treatments.

Where is the study run from?
The study was run from Selkirk College Castlegar British Columbia Canada, but recruitment, treatment and data collection were only run at one location, ProMedica Sports Care (primary care) facility in Toledo Ohio USA.

When is the study starting and how long is it expected to run for?
We began recruitment September 01, 2009 and completed the last follow up evaluations January 28, 2011. We recruited subjects for 4 months up until December 31, 2009.

Who is funding the study?
The study was funded by the manufacturer of the laser, LiteCure LLT, but they were not involved in the study design or in the analysis and reporting of any of the data.

Who is the main contact?
Dr. Delia Roberts
Ethics approval ProMedica Health System Institutional Review Board. #09-005. Approval received July 29, 2009. Continuation received January 29, 2010.
Study design Randomized double blinded placebo controlled clinical trial
Countries of recruitment Canada
Disease/condition/study domain Tendinopathy of the extensor carpi radialis brevis tendon
Participants - inclusion criteria 1. Adults (between the ages of 18 and 65 years of age), either sex
2. Diagnosis of epicondylitis due to injury to the extensor carpi radialis brevis tendon
Participants - exclusion criteria 1. Individuals with tattoos, melanoma or pigmented areas around the treatment area
2. Those taking corticosteroids
3. Pregnant
4. With hemorrhagic or cardiac disease
5. Photosensitivity
6. Individuals who had the extensor carpi radialis brevis tendon injected within 3 months prior to the study were also excluded to ensure that there was no influence of prior treatment on the current investigation.
Anticipated start date 01/09/2009
Anticipated end date 28/01/2011
Status of trial Completed
Patient information material Not available in web format, please use contact details below to request a patient information sheet
Target number of participants 15
Interventions The area to be treated was demarcated at ½ the distance from the lateral epicondyle to the ulnar styloid process and 1/3 of the distance from the lateral epicondyle to the acromion process. The laser probe was kept perpendicular to, and approximately 2.5 cm above the surface of the dermis, creating a spot size 5.7 - 9.6 cm2. The laser was set at full power (600J/min) with a continuous wave form generating a total dose per treatment of 3000 J in 5 min or 6.6 ± 1.3 J/cm2. The first 2.5 minutes of the laser treatment were administered with the arm in full extension, and the second 2.5 minutes were administered while passively moving the joint through its range of motion. Half of the treatment was delivered along the long axis to the tendon, with the other half delivered transverse to the tendon while covering the anterior, lateral and posterior aspects of the lateral epicondyle.

The treatment schedule was as follows: three treatments on consecutive days, four additional treatments over the next ten days and one final treatment during the third week.

The placebo control instrument was a sham machine which appeared identical to the true laser in every way, however the laser had been disabled and only the aiming beam (incandescent light) was functioning.
Primary outcome measure(s) The primary outcome measures included both subjective and objective measures to indicate a restoration of strength and function of the extensor carpi radialis brevis tendon from pre-treatment to pre-injury levels. All evaluations were performed by blinded Sport Medicine physicians pre-treatment (baseline), immediately post-completion of the treatment series, and again at three months, six months and 12 months post-treatment. These measures included:
1. Reduction in the rating of pain at rest on using the Visual Analogue Scale (VAS) score (0 = no pain, 10 = unbearable pain)
2. Increased strength on extension (scale of 1-5 with 5 being full strength), and strength on flexion from three maximal trials using the using the Smedley III Digital Grip Strength Tester (in kg)
3. Pain during maximal contractions was also rated using the VAS 10-point scale
Secondary outcome measure(s) No secondary outcome measures
Sources of funding LiteCure LLC (USA)
Trial website
Publications 2013 results in: http://www.ncbi.nlm.nih.gov/pubmed/23733499
Contact name Dr  Delia  Roberts
  Address Biology
Selkirk College
301 Frank Beinder Way
  City/town Castlegar British Columbia
  Zip/Postcode V1N 4L3
  Country Canada
Sponsor ProMedica Health Systems Sports Care (USA)
  Address c/o Dr. Roger Kruse
Sports Care
Wildwood Medical Center
2865 N. Reynolds Road, Ste. 110
  City/town Toledo Ohio
  Zip/Postcode 43615
  Country United States of America
  Sponsor website: http://www.promedica.org/sportscare
Date applied 09/01/2013
Last edited 24/02/2014
Date ISRCTN assigned 16/01/2013
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