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Comparison of Platelet Rich Plasma and Alternative Therapies for the Treatment of Tennis Elbow (Lateral Epicondylitis) (IMPROVE)

Primary Purpose

Lateral Epicondylitis (Tennis Elbow)

Status
Terminated
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Platelet Rich Plasma (PRP) Injection
Whole Blood Injection
Dry Needle Fenestration
Sham Injection
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lateral Epicondylitis (Tennis Elbow) focused on measuring Lateral Epicondylitis, Tennis Elbow, Platelet Rich Plasma, Whole Blood, Tendon Fenestration

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult man or woman aged 18 years or greater.
  • Clinical diagnosis of lateral epicondylitis based on site of pain, pain elicited with active extension of the wrist in pronation and elbow extension.
  • Documented sonographic diagnosis of common extensor tendinosis based on tendon thickening, areas of hypoechogenicity, and loss of the normal echotexture.
  • Chronic symptoms (equal or greater than 3 months).
  • Pain of at least 5 out of 10 on a visual analog scale (VAS).
  • Provision of informed consent.

Exclusion Criteria:

  • Acute symptom onset (less than 2 months).
  • History of acute elbow trauma (less than one week).
  • History of rheumatoid arthritis.
  • History of malignancy.
  • Pregnancy
  • Patients requiring anti-platelet medication for the treatment of heart attack, stroke or other medical condition.
  • Previous surgery for lateral epicondylitis.
  • Previous local injections, including steroids within the past 6 months.
  • Signs of other causes for lateral elbow pain (posterior interosseous nerve entrapment, osteochondral lesion).

Sites / Locations

  • University of Michigan
  • Hamilton General Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Platelet Rich Plasma (PRP) Injection

Whole Blood Injection

Dry Needle Fenestration

Sham Injection

Arm Description

Patients in this arm will receive a platelet rich plasma injection at the site of their lateral epicondylitis, followed by post-treatment physical therapy exercises.

Patients in this arm will receive a whole blood injection at the site of their lateral epicondylitis, followed by post-treatment physical therapy exercises.

Patients in this arm will receive 15-25 gentle strokes of dry needling (piercing of the tendon) at the site of their lateral epicondylitis, followed by post-treatment physical therapy exercises. No blood will be injected into the tendon.

Patients in this arm will receive a sham injection, followed by post-treatment physical therapy exercises. No blood will be injected into the tendon.

Outcomes

Primary Outcome Measures

Pain Reduction
Pain reduction will be measured using the Visual Analog Scale (VAS), a subjective scale in which the patient rates their pain on a scale from 0 to 10 (0, no pain, 10, maximum possible pain).

Secondary Outcome Measures

Functional Disability
Functional disability will be measured using the Liverpool Elbow Score (LES) which is an assessment tool for evaluating function based on range of motion, ulnar nerve function, and ability to perform daily activities.
Psychological Impairment
Psychological impairment (depression and anxiety) will be assessed using the Hospital Anxiety and Depression Scale (HADS) which is a reliable, validated, and practical tool for identifying and quantifying anxiety and depression.
Health-Related Quality of Life
Health-related quality of life will be measured using the 12-Item Short Form Health Survey (SF-12).

Full Information

First Posted
August 16, 2012
Last Updated
April 6, 2023
Sponsor
McMaster University
Collaborators
Arthrex, Inc., The Physicians' Services Incorporated Foundation, Radiological Society of North America
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1. Study Identification

Unique Protocol Identification Number
NCT01668953
Brief Title
Comparison of Platelet Rich Plasma and Alternative Therapies for the Treatment of Tennis Elbow (Lateral Epicondylitis)
Acronym
IMPROVE
Official Title
Impact of Platelet Rich Plasma Over Alternative Therapies in Patients With Lateral Epicondylitis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Terminated
Why Stopped
Did not analyze data
Study Start Date
August 2012 (undefined)
Primary Completion Date
April 2023 (Actual)
Study Completion Date
April 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
Arthrex, Inc., The Physicians' Services Incorporated Foundation, Radiological Society of North America

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
"Tennis elbow" is the most common cause of lateral elbow pain, generally caused by either work or sports related repetitive strain. In this condition, a tendon along the outside of the elbow becomes inflamed leading to pain, especially with flexing and extending the elbow. Many treatments have been attempted, including physiotherapy and steroids, with little success. One treatment which has been very effective is the injection of the patients own blood (taken from their other non-affected arm) into their abnormal tendon. The blood recruits the patients own healing factors and heals the damaged tendon. As platelets are thought to be largely responsible, injection of concentrated platelets, extracted from the patient's blood (platelet rich plasma) is a newer, but expensive, technique. At this point, it is unclear whether whole blood, concentrated platelets, or simply passing a ultrasound-guided needle through the abnormal tendon as a means to stimulate tissue healing (tendon fenestration) is the better treatment. The objective of this trial is to compare platelet rich plasma, whole blood, dry needle tendon fenestration, and sham injection (with physical therapy) to identify the best and most cost-effective therapy for this debilitating condition.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lateral Epicondylitis (Tennis Elbow)
Keywords
Lateral Epicondylitis, Tennis Elbow, Platelet Rich Plasma, Whole Blood, Tendon Fenestration

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Platelet Rich Plasma (PRP) Injection
Arm Type
Experimental
Arm Description
Patients in this arm will receive a platelet rich plasma injection at the site of their lateral epicondylitis, followed by post-treatment physical therapy exercises.
Arm Title
Whole Blood Injection
Arm Type
Active Comparator
Arm Description
Patients in this arm will receive a whole blood injection at the site of their lateral epicondylitis, followed by post-treatment physical therapy exercises.
Arm Title
Dry Needle Fenestration
Arm Type
Active Comparator
Arm Description
Patients in this arm will receive 15-25 gentle strokes of dry needling (piercing of the tendon) at the site of their lateral epicondylitis, followed by post-treatment physical therapy exercises. No blood will be injected into the tendon.
Arm Title
Sham Injection
Arm Type
Placebo Comparator
Arm Description
Patients in this arm will receive a sham injection, followed by post-treatment physical therapy exercises. No blood will be injected into the tendon.
Intervention Type
Other
Intervention Name(s)
Platelet Rich Plasma (PRP) Injection
Intervention Description
The subcutaneous soft tissues of the lateral elbow will be infiltrated with 1% lidocaine for local anesthetic. A 22-gauge needle will then be placed into the tendon followed by 15-25 gentle strokes of dry needling in which the needle pierces the tendon at multiple sites. For the PRP preparation, the Arthrex ACP system will be used. This is a closed, double syringe system which uses 16 mL of whole blood drawn from the patient's contralateral arm, using a 19G butterfly needle. The blood is centrifuged at 1500 rpm for 5 minutes and extracts 4-7 ml of PRP. No anticoagulant will be used. Fenestration of the tendon will continue as 3mL of PRP is injected into the common extensor tendon. The remaining PRP will be sent for analysis of platelet, WBC, and RBC concentrations.
Intervention Type
Other
Intervention Name(s)
Whole Blood Injection
Intervention Description
The subcutaneous soft tissues of the lateral elbow will be infiltrated with 1% lidocaine for local anesthetic. A 22-gauge needle will then be placed into the tendon followed by 15-25 gentle strokes of dry needling in which the needle pierces the tendon at multiple sites. 6mL of autologous whole blood will be drawn from the patient's contralateral arm, using a 19G butterfly needle. Fenestration of the tendon will continue as 3mL of whole blood biologic agent is injected into the common extensor tendon. The remaining 3mL will be sent for analysis of platelet, WBC, and RBC concentrations.
Intervention Type
Other
Intervention Name(s)
Dry Needle Fenestration
Intervention Description
The subcutaneous soft tissues of the lateral elbow will be infiltrated with 1% lidocaine for local anesthetic. 3mL of autologous whole blood will be drawn from the patient's contralateral arm, using a 19G butterfly needle, and discarded. A 22-gauge needle will then be placed into the tendon. 15-25 strokes or as many strokes required until tendon is softened of dry needling will be performed in which the needle pierces the tendon at multiple sites. No blood will be injected into the tendon.
Intervention Type
Other
Intervention Name(s)
Sham Injection
Intervention Description
The subcutaneous soft tissues of the lateral elbow will be infiltrated with 1% lidocaine (no epinephrine) for local anesthetic. 3mL of autologous whole blood will be drawn from the patient's contralateral arm, using a 19G butterfly needle, and discarded. The superficial subcutaneous soft tissues will be re-entered however, the tendon itself will not be entered and nothing will be injected.
Primary Outcome Measure Information:
Title
Pain Reduction
Description
Pain reduction will be measured using the Visual Analog Scale (VAS), a subjective scale in which the patient rates their pain on a scale from 0 to 10 (0, no pain, 10, maximum possible pain).
Time Frame
Baseline, 6 weeks, 3, 6, 12 months
Secondary Outcome Measure Information:
Title
Functional Disability
Description
Functional disability will be measured using the Liverpool Elbow Score (LES) which is an assessment tool for evaluating function based on range of motion, ulnar nerve function, and ability to perform daily activities.
Time Frame
Baseline, 6 weeks, 3, 6, 12, 24 months
Title
Psychological Impairment
Description
Psychological impairment (depression and anxiety) will be assessed using the Hospital Anxiety and Depression Scale (HADS) which is a reliable, validated, and practical tool for identifying and quantifying anxiety and depression.
Time Frame
Baseline, 6 weeks, 3, 6, 12, 24 months
Title
Health-Related Quality of Life
Description
Health-related quality of life will be measured using the 12-Item Short Form Health Survey (SF-12).
Time Frame
Baseline, 6 weeks, 3, 6, 12, 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult man or woman aged 18 years or greater. Clinical diagnosis of lateral epicondylitis based on site of pain, pain elicited with active extension of the wrist in pronation and elbow extension. Documented sonographic diagnosis of common extensor tendinosis based on tendon thickening, areas of hypoechogenicity, and loss of the normal echotexture. Chronic symptoms (equal or greater than 3 months). Pain of at least 5 out of 10 on a visual analog scale (VAS). Provision of informed consent. Exclusion Criteria: Acute symptom onset (less than 2 months). History of acute elbow trauma (less than one week). History of rheumatoid arthritis. History of malignancy. Pregnancy Patients requiring anti-platelet medication for the treatment of heart attack, stroke or other medical condition. Previous surgery for lateral epicondylitis. Previous local injections, including steroids within the past 6 months. Signs of other causes for lateral elbow pain (posterior interosseous nerve entrapment, osteochondral lesion).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mary M Chiavaras, MD, PhD
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109-5326
Country
United States
Facility Name
Hamilton General Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
34590307
Citation
Karjalainen TV, Silagy M, O'Bryan E, Johnston RV, Cyril S, Buchbinder R. Autologous blood and platelet-rich plasma injection therapy for lateral elbow pain. Cochrane Database Syst Rev. 2021 Sep 30;9(9):CD010951. doi: 10.1002/14651858.CD010951.pub2.
Results Reference
derived

Learn more about this trial

Comparison of Platelet Rich Plasma and Alternative Therapies for the Treatment of Tennis Elbow (Lateral Epicondylitis)

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