Efficacy of Injection Therapy for Lateral Epicondylosis

NCT ID: NCT01476605

Last Updated: 2019-02-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 31 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-06-30
• Study Completion Date: 2015-12-01

Brief Summary

While evidence does not identify any conventional therapy as definitive for chronic lateral epicondylosis (CLE, tennis elbow), basic science and limited pilot level trials support rigorous assessment of prolotherapy (PrT) and platelet-rich plasma (PRP) as therapy for CLE. The proposed study will conduct a pilot RCT assessing 2 PrT solutions and PRP injections commonly used in the treatment of moderate-to-severe tennis elbow using clinical, biomechanical and radiological outcomes. Data from this study will support a future confirmatory study to find an effective treatment for moderate-to-severe tennis elbow. In support of this goal, the investigators propose the following research questions.

Does PrT or PRP, compared to waitlist control:

1. improve pain- and function-dependent, CLE-specific quality of life among adults with CLE, as assessed by a validated questionnaire, the elbow-specific Patient-Rated Tennis Elbow Evaluation?

2. improve upper extremity performance among adults with CLE as assessed by a blinded assessor using elbow-specific, effort-dependent biomechanical measures of grip strength (pain-free and maximal), stiffness, effective mass and damping

3. improve the radiologic appearance of several pathologic features of CLE as evaluated using imaging studies of lateral elbow structures: ultrasound to assess a) neovascularity (color Doppler), b) hypoechogenicity (grayscale US), and c) tendon stiffness ("acousto-elastic strain gauge" technique) using standardized, 0-3 severity scales, and d) MRI to assess the overall common extensor tensor tendon disease severity using a standardized 0-3 scale?

4. provide satisfying treatment to subjects as assessed by a treatment satisfaction survey and a qualitative exit interview?

Detailed Description

CLE is a prevalent, disabling condition with significant individual and societal costs. The incidence of CLE is increasing. CLE is often refractory to care. There is limited scientific evidence to support specific therapies.

PrT and PRP show promise as effective therapy for CLE that can be performed in the primary care setting. Pilot-level RCTs of PrT and PRP for CLE have reported large absolute effect sizes. Findings from invitro and animal studies are consistent with the results of clinical trials and suggest that both therapies can improve clinical outcomes and modify disease in CLE. However, prior research is limited by lack of methodological rigor, non-validated outcome measures and lack of integrated multidisciplinary outcome measures.

Positive trends in the proposed study would suggest the effect size of PrT and PRP for CLE, and allow the calculation of a robust sample size to power an R01 study, and pilot test the use of an integrated set of outcome measures. Statistically significant positive results on clinical, biomechanical and radiological outcomes would demonstrate that PrT and PRP can treat, modify the disease of and may be a cure for CLE. Such findings would provide enormous benefits to patients through improved quality of life, reduced pain and disability, and to industry and society at large through reduced workers' injury claims and absenteeism.

Conditions

Tennis Elbow

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: FACTORIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

PrT-DMS

1.0 mL 5% morrhuate sodium + 1.5 mL 50% dextrose, 1 mL 2% lidocaine and 3.5 mL normal saline.

Group Type: ACTIVE_COMPARATOR

PrT-DMS

Intervention Type: PROCEDURE

PrT-DMS. 1.0 mL 5% morrhuate sodium + 1.5 mL 50% dextrose, 1 mL 2% lidocaine and 3.5 mL normal saline.

PrT-D

PrT-D solution is 4 mL 50% dextrose, 3 mL normal saline, and 2 mL 2% lidocaine

Group Type: EXPERIMENTAL

Dextrose prolotherapy

Intervention Type: PROCEDURE

PrT-D solution is 4 mL 50% dextrose, 3 mL normal saline, and 2 mL 2% lidocaine

Waitlist

Group Type: NO_INTERVENTION

No interventions assigned to this group

Platelet rich plasma

Group Type: ACTIVE_COMPARATOR

Platelet Rich Plasma injection

Intervention Type: PROCEDURE

Platelet rich plasma injection therapy (PRP) uses components of autologous blood to promote healing in chronically diseased joint tissues.

Interventions

Dextrose prolotherapy

PrT-D solution is 4 mL 50% dextrose, 3 mL normal saline, and 2 mL 2% lidocaine

Intervention Type: PROCEDURE

PrT-DMS

PrT-DMS. 1.0 mL 5% morrhuate sodium + 1.5 mL 50% dextrose, 1 mL 2% lidocaine and 3.5 mL normal saline.

Intervention Type: PROCEDURE

Platelet Rich Plasma injection

Platelet rich plasma injection therapy (PRP) uses components of autologous blood to promote healing in chronically diseased joint tissues.

Intervention Type: PROCEDURE

Other Intervention Names

dextrose; Dextrose and Morrhuate sodium PrT; Platelet rich plasma

Eligibility Criteria

Inclusion Criteria

1. age 18-65 years

2. diagnosis of CLE, confirmed by the PI using clinical symptoms and exam findings of tenderness over the lateral epicondyle and/or extensor tendon, and pain on 2 extensor muscle provocation tests

3. self-reported CLE-related pain for at least 6 months

4. self-reported failure of at least 2 of the 3 most common treatments for CLE (a course of NSAIDS, physical therapy or corticosteroid injections).

Exclusion Criteria

1. current bilateral CLE

2. a corticosteroid injection in the prior 3 months or prior PrT or PRP for CLE

3. current carpal tunnel syndrome, other elbow pathology, or acute trauma of the CLE-affected upper extremity

4. self-reported history of bleeding disorders, other hematologic conditions, inflammatory arthritis, systemic nervous system disease, upper extremity surgeries or neuropathy

5. current use of opioids for pain

6. anticoagulation or immunosuppressive therapy in the prior month

7. intent to use NSAIDs or steroids

8. known allergy to dextrose, acetaminophen or lidocaine

9. MRI contraindications: non-compatible metal in the CLE-affected upper extremity or severe claustrophobia

10. unresolved litigation

11. self-reported pregnancy. Pregnant women are excluded from the study because pregnancy changes the characteristics of connective tissue including ligaments and tendons associated with CLE and, so, is an unacceptable confounder in this pilot level study. There is no report however, about dextrose, morrhuate sodium or PrT being harmful to pregnant women. Therefore we will not draw confirmatory labs to ensure that women of childbearing age are not pregnant. Rather we will accept self-report on pregnancy status at the time of consent. If a woman becomes pregnant during the study she will be dropped from the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Wisconsin, Madison

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

David P Rabago, MD

Role: PRINCIPAL_INVESTIGATOR

University of Wisconsin, Department of Family Medicine

John Wilson, MD

Role: PRINCIPAL_INVESTIGATOR

UW Dept of Family Medicine

Locations

Northeast Family Medical Center

Madison, Wisconsin, United States

University of Wisconsin General Clinical Research Center

Madison, Wisconsin, United States

Countries

United States

Related Links

http://www.fammed.wisc.edu

University of Wisconsin Department of Family Medicine

Other Identifiers

G0810

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

H-2008-0148

Identifier Type: -

Identifier Source: org_study_id