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Completed

NCT Number: NCT03978897

Trial of Blood Flow Restriction Plus Physical Therapy vs. Physical Therapy Alone for Lateral Epicondylitis

Open label randomized controlled trial comparing evidenced based physical/occupational therapy vs. physical/occupational therapy including blood flow restriction tourniquet in the treatment of lateral epicondylitis (tennis elbow).

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cleveland Clinic Akron General

Akron, Ohio, 44307, United States

About this study

Patients will be randomized to one of two groups, and treatment will be open label and unblinded. A target of 44 patients for enrollment has been set for 80% power, actual enrollment resulted in 41 patients undergoing randomization. Treatment will last for 6 visits with physical therapy with recommended visit intervals of 1 week :

Intervention Group: Evidence based physical/occupational therapy, with the addition of therapeutic exercises using a blood flow restriction tourniquet.

Control Group: Patients will receive standard evidence based physical therapy

The primary outcome (Patient-Rated Tennis Elbow Evaluation [PRTEE]) will be collected at enrollment, 3, 6, and 12 months.

Secondary outcomes will be collected at the beginning and end of physical therapy interventions (change in: numeric pain rating scale, maximum pain free grip strength, pain free grip strength). We will collect treatments received after the end of physical therapy and before final follow up.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The diagnoses included are lateral elbow pain, lateral epicondylitis, or lateral epicondylalgia, more general diagnoses elbow tendinitis or elbow pain will be included if their clinical picture at physical therapy meets criteria for lateral epicondylitis.
  • If the inclusion diagnosis is other than lateral epicondylitis or tennis elbow (such as elbow pain), we will confirm the diagnosis at the first therapy visit with tenderness at the lateral epicondyle and/or pain with resisted wrist/long finger extension at the lateral epicondyle.
  • Pain for 4 weeks or more.
  • All participants must be between the age of 18 and 70 years old and have had pain for 4 weeks or more.

Exclusion criteria

  • Ligamentous elbow sprain, osteoarthritis of elbow and cervical radiculopathy in the affected limb will be excluded from the study.
  • Any history of ligamentous, bony or other soft tissue reconstruction surgery at the affected elbow,
  • Vascular disorders to include: history of DVT, history of endothelial dysfunction, peripheral vascular disease
  • Injection therapy (corticosteroid, platelet rich plasma, or other injection therapy) in the prior 3 months to the affected site
  • Current fracture in affected arm
  • History of crush injury to affected arm
  • Any surgery on affected arm in last 1 year
  • Surgical procedure on their contralateral extremity (Changed 9/2019 to surgery within last year on contralateral upper extremity).
  • History of lymphectomy (such as axillary exploration with breast surgery, lymph node biopsy in the affected axilla/arm)
  • Pregnancy
  • Active infection
  • Current cancer diagnosis/treatment
  • Sickle cell anemia or trait
  • Kidney dialysis
  • History of syncope/passing out with pressure to body (such as massage, or blood pressure cuff).
  • inability to consent

Treatment and study plan

Blood flow restriction tourniquet

Device

A blood flow restriction tourniquet, which impedes arterial flow to extremity at 50% of usual flow.

Other names: Delfi personalized tourniquet system

Evidence based physical/occupational therapy

Other

Up to date physical/occupational therapy for lateral epicondylitis

Primary outcomes

  1. Change in Patient Rated Tennis Elbow Evaluation (PRTEE)

    Time frame: 12 months

    Change in score on 'Patient rated tennis elbow evaluation' total score from baseline to 12 month final follow up. Lower numbers suggest less pain, higher scores suggest more pain. Total score 0-100.

    Includes pain subscale (0-50)

    Specific activities subscale (0-60)

    Usual activities subscale (0-40)

    Function Subscale= (specific activities score + usual activities score)/2 (0-50)

    Total Score= Pain subscale + Function Subscale (0-100)

Secondary outcomes

  1. Numeric Pain Rating Scale

    Time frame: 12 months

    change in score from baseline to final 12 month follow up on 0-10 pain rating scale with 0 being no pain, and 10 being worst pain.

  2. Pain Free Grip Strength

    Time frame: at final therapy visit up to 12 weeks after enrollment

    Change in pain free grip strength (kg) on dynamometer from baseline to final PT visit (approximately 12 weeks)

  3. Maximum Grip Strength

    Time frame: at final therapy visit up to 12 weeks after enrollment

    Change in maximum grip strength (kg) on dynamometer from baseline visit to final PT visit (approximately 12 weeks)

  4. Other Treatments Received

    Time frame: 12 months

    We will collect data on whether the patient sought or received treatments beyond physical/occupational therapy over the 12 months of enrollment in the study

Sponsors and collaborators

Lead sponsor

Cleveland Clinic Akron General

Other

Registry information

Official study title

A Randomized Controlled Trial of Blood Flow Restriction Plus Conventional Physical Therapy vs. Conventional Physical Therapy Alone in the Treatment of Lateral Epicondylitis

Important dates

Study start
2019
Primary completion
2024
Study completion
2024
First posted
Jun 7, 2019
Registry last updated
May 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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