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PRP Versus Saline in Lateral Epicondylitis

Primary Purpose

Lateral Epicondylitis, Unspecified Elbow

Status
Not yet recruiting
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Platelet rich plasma injection
Saline injection
Sponsored by
Singapore General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lateral Epicondylitis, Unspecified Elbow focused on measuring platelet rich plasma, saline, randomised controlled trial

Eligibility Criteria

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

Inclusion Criteria:

  • Patients of age >21 years old
  • History of chronic pain on the lateral side of the elbow and pain on lateral epicondyle on direct palpation and resisted dorsiflexion of the wrist for more than 3 months
  • Ability of patients to provide informed consent

Exclusion Criteria:

  • Previous tennis elbow surgery to affected elbow
  • Previous corticosteroid injections to affected elbow
  • Concurrent complementary and alternative medicine (CAM) treatments e.g. acupuncture
  • Inflammatory diseases / infection / fracture / trauma
  • Neck pain on ipsilateral side
  • Chronic pain syndromes
  • Malignancies
  • Pregnant or lactating females
  • Consistent use of NSAIDs within 48 hours of procedure
  • Systemic use of corticosteroids within 2 weeks
  • History of anemia, any blood disorders, hypothyroidism

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Platelet rich plasma injection

    Saline injection

    Arm Description

    Patients will be treated with a single PRP injection, where 8 mL of whole blood will be collected and 2.5 mL of PRP will be given to the patient. Routine physiotherapy regimens will be implemented, similar to placebo arm.

    Patients will be treated with 2.5 mL saline 0.9%. Routine physiotherapy regimens will be implemented, similar to intervention arm.

    Outcomes

    Primary Outcome Measures

    Patient-Related Tennis Elbow Evaluation (PRTEE) pain in affected arm
    Rates pain from 0 (no pain) to 10 (worst imaginable) for at rest, doing task with repeated arm movement, carrying plastic bag of groceries, when pain was least, when pain was worst
    Patient-Related Tennis Elbow Evaluation (PRTEE) pain in affected arm
    Rates pain from 0 (no pain) to 10 (worst imaginable) for at rest, doing task with repeated arm movement, carrying plastic bag of groceries, when pain was least, when pain was worst
    Patient-Related Tennis Elbow Evaluation (PRTEE) pain in affected arm
    Rates pain from 0 (no pain) to 10 (worst imaginable) for at rest, doing task with repeated arm movement, carrying plastic bag of groceries, when pain was least, when pain was worst
    Patient-Related Tennis Elbow Evaluation (PRTEE) pain in affected arm
    Rates pain from 0 (no pain) to 10 (worst imaginable) for at rest, doing task with repeated arm movement, carrying plastic bag of groceries, when pain was least, when pain was worst
    Patient-Related Tennis Elbow Evaluation (PRTEE) functional disability
    Rates from 0 (no difficulty) to 10 (unable to do) on specific activities and usual activities. Specific activities include turning doorknob or key, carrying grocery bag or briefcase by handle, lifting full coffee cup or glass of milk to mouth, opening jars, pulling up pants, wringing out washcloths or wet towels. Usual activities include personal activities (dressing, washing), household work (cleaning, maintenance), work (job), recreational or sporting activities.
    Patient-Related Tennis Elbow Evaluation (PRTEE) functional disability
    Rates from 0 (no difficulty) to 10 (unable to do) on specific activities and usual activities. Specific activities include turning doorknob or key, carrying grocery bag or briefcase by handle, lifting full coffee cup or glass of milk to mouth, opening jars, pulling up pants, wringing out washcloths or wet towels. Usual activities include personal activities (dressing, washing), household work (cleaning, maintenance), work (job), recreational or sporting activities.
    Patient-Related Tennis Elbow Evaluation (PRTEE) functional disability
    Rates from 0 (no difficulty) to 10 (unable to do) on specific activities and usual activities. Specific activities include turning doorknob or key, carrying grocery bag or briefcase by handle, lifting full coffee cup or glass of milk to mouth, opening jars, pulling up pants, wringing out washcloths or wet towels. Usual activities include personal activities (dressing, washing), household work (cleaning, maintenance), work (job), recreational or sporting activities.
    Patient-Related Tennis Elbow Evaluation (PRTEE) functional disability
    Rates from 0 (no difficulty) to 10 (unable to do) on specific activities and usual activities. Specific activities include turning doorknob or key, carrying grocery bag or briefcase by handle, lifting full coffee cup or glass of milk to mouth, opening jars, pulling up pants, wringing out washcloths or wet towels. Usual activities include personal activities (dressing, washing), household work (cleaning, maintenance), work (job), recreational or sporting activities.
    Visual analog scale (VAS) pain with resisted wrist extension
    Rated from 0 (no pain) to 5 (extremely pain)
    Visual analog scale (VAS) pain with resisted wrist extension
    Rated from 0 (no pain) to 5 (extremely pain)
    Visual analog scale (VAS) pain with resisted wrist extension
    Rated from 0 (no pain) to 5 (extremely pain)
    Visual analog scale (VAS) pain with resisted wrist extension
    Rated from 0 (no pain) to 5 (extremely pain)
    Visual analog scale (VAS) pain with contraction of extensor carpi radialis brevis and extensor digitorum communis
    Rated from 0 (no pain) to 5 (extremely pain)
    Visual analog scale (VAS) pain with contraction of extensor carpi radialis brevis and extensor digitorum communis
    Rated from 0 (no pain) to 5 (extremely pain)
    Visual analog scale (VAS) pain with contraction of extensor carpi radialis brevis and extensor digitorum communis
    Rated from 0 (no pain) to 5 (extremely pain)
    Visual analog scale (VAS) pain with contraction of extensor carpi radialis brevis and extensor digitorum communis
    Rated from 0 (no pain) to 5 (extremely pain)
    Ultrasound tendon
    Ultrasonographic changes in tendon thickness and color Doppler activity will be recorded
    Ultrasound tendon
    Ultrasonographic changes in tendon thickness and color Doppler activity will be recorded

    Secondary Outcome Measures

    Full Information

    First Posted
    October 23, 2021
    Last Updated
    November 6, 2021
    Sponsor
    Singapore General Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05125705
    Brief Title
    PRP Versus Saline in Lateral Epicondylitis
    Official Title
    Treatment of Lateral Epicondylitis With Platelet-Rich Plasma Versus Saline: A Double-Blinded Randomized Placebo-Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2021
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    November 2021 (Anticipated)
    Primary Completion Date
    May 2022 (Anticipated)
    Study Completion Date
    November 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Singapore General Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Lateral epicondylitis (LE), also known as tennis elbow, has an estimated prevalence in the general population of 1% to 3%, peaking at age 45 years to 54 years and affect both men and women equally. A randomised controlled trial published in The Lancet showed that 83% of the patients suffering from LE of more than 6 weeks duration on wait-and-see policy recovered only after 1 year without any therapeutic interventions. The costs associated with LE is substantial as patients not only incur hefty healthcare costs but also lose their productivity owing to their long recovery period. Currently, there is a paucity of evidence worldwide for the efficacy of PRP injections compared to control in LE. This randomised controlled trial aims to compare the efficacy of PRP versus placebo (saline) injections in adults with LE.
    Detailed Description
    The pathogenesis of LE was initially believed to be a generalised inflammatory process. However, in 1979, the pathology was better understood as invading immature fibroblasts disorganizing the normal collagen architecture of the elbow, associated with immature vascular responses to cellular repair. There is a variety of treatment modalities available for LE, varying from watchful waiting without any therapeutic interventions, pharmaceutical methods such as prescribing non-steroidal anti-inflammatory drugs, physiotherapy such as encouraging bracing and exercise, injections, and surgical modalities once non-surgical options fail. For many years, injection with glucocorticoids has remained the mainstay of treatment. However, several studies have proven that the effects of corticosteroid injections do not seem to last in the long-term, amongst which a trial published in The Lancet showed that long-term differences at 52 weeks between injections and physiotherapy was significantly in favour of physiotherapy. Recently, many studies worldwide have demonstrated that platelet-rich-plasma (PRP) stimulates cartilage repair by actively secreting growth factors which activate cell proliferation and differentiation thereby promoting tissue regeneration. It has been postulated that PRP stimulates repair mechanisms within tendons and hence promote tendon healing. However, there is a paucity of evidence worldwide for the efficacy of PRP injections compared to control in LE. Currently, PRP treatment is not formally recognized as a treatment modality for LE in Singapore, with the accepted indications for PRP treatment being limited to non-surgical treatment of acute muscle and ligamentous injuries, and the biological augmentation of acute Achilles tendon repairs. This randomised controlled trial aims to compare the efficacy of PRP versus placebo (saline) injections in adults with LE.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Lateral Epicondylitis, Unspecified Elbow
    Keywords
    platelet rich plasma, saline, randomised controlled trial

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2, Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantOutcomes Assessor
    Masking Description
    Both the patients and the outcome assessor will be blinded in this trial.
    Allocation
    Randomized
    Enrollment
    70 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Platelet rich plasma injection
    Arm Type
    Experimental
    Arm Description
    Patients will be treated with a single PRP injection, where 8 mL of whole blood will be collected and 2.5 mL of PRP will be given to the patient. Routine physiotherapy regimens will be implemented, similar to placebo arm.
    Arm Title
    Saline injection
    Arm Type
    Placebo Comparator
    Arm Description
    Patients will be treated with 2.5 mL saline 0.9%. Routine physiotherapy regimens will be implemented, similar to intervention arm.
    Intervention Type
    Biological
    Intervention Name(s)
    Platelet rich plasma injection
    Other Intervention Name(s)
    PRP
    Intervention Description
    The PRP is prepared by RegenLab's RegenKit-THT, in accordance with operating instructions supplied with the kit. The device allows automated blood collection (8 mL) and blood component separation in closed circuit. After centrifugation at room temperature for 9 minutes at centrifugal force of 1500g, the RegenTHT tube is then inverted several times before re-suspension, allowing 4mL of PRP to be obtained for each tube. 2.5mL will be injected into patients
    Intervention Type
    Other
    Intervention Name(s)
    Saline injection
    Intervention Description
    Saline injection
    Primary Outcome Measure Information:
    Title
    Patient-Related Tennis Elbow Evaluation (PRTEE) pain in affected arm
    Description
    Rates pain from 0 (no pain) to 10 (worst imaginable) for at rest, doing task with repeated arm movement, carrying plastic bag of groceries, when pain was least, when pain was worst
    Time Frame
    baseline
    Title
    Patient-Related Tennis Elbow Evaluation (PRTEE) pain in affected arm
    Description
    Rates pain from 0 (no pain) to 10 (worst imaginable) for at rest, doing task with repeated arm movement, carrying plastic bag of groceries, when pain was least, when pain was worst
    Time Frame
    6 weeks
    Title
    Patient-Related Tennis Elbow Evaluation (PRTEE) pain in affected arm
    Description
    Rates pain from 0 (no pain) to 10 (worst imaginable) for at rest, doing task with repeated arm movement, carrying plastic bag of groceries, when pain was least, when pain was worst
    Time Frame
    3 months
    Title
    Patient-Related Tennis Elbow Evaluation (PRTEE) pain in affected arm
    Description
    Rates pain from 0 (no pain) to 10 (worst imaginable) for at rest, doing task with repeated arm movement, carrying plastic bag of groceries, when pain was least, when pain was worst
    Time Frame
    6 months
    Title
    Patient-Related Tennis Elbow Evaluation (PRTEE) functional disability
    Description
    Rates from 0 (no difficulty) to 10 (unable to do) on specific activities and usual activities. Specific activities include turning doorknob or key, carrying grocery bag or briefcase by handle, lifting full coffee cup or glass of milk to mouth, opening jars, pulling up pants, wringing out washcloths or wet towels. Usual activities include personal activities (dressing, washing), household work (cleaning, maintenance), work (job), recreational or sporting activities.
    Time Frame
    baseline
    Title
    Patient-Related Tennis Elbow Evaluation (PRTEE) functional disability
    Description
    Rates from 0 (no difficulty) to 10 (unable to do) on specific activities and usual activities. Specific activities include turning doorknob or key, carrying grocery bag or briefcase by handle, lifting full coffee cup or glass of milk to mouth, opening jars, pulling up pants, wringing out washcloths or wet towels. Usual activities include personal activities (dressing, washing), household work (cleaning, maintenance), work (job), recreational or sporting activities.
    Time Frame
    6 weeks
    Title
    Patient-Related Tennis Elbow Evaluation (PRTEE) functional disability
    Description
    Rates from 0 (no difficulty) to 10 (unable to do) on specific activities and usual activities. Specific activities include turning doorknob or key, carrying grocery bag or briefcase by handle, lifting full coffee cup or glass of milk to mouth, opening jars, pulling up pants, wringing out washcloths or wet towels. Usual activities include personal activities (dressing, washing), household work (cleaning, maintenance), work (job), recreational or sporting activities.
    Time Frame
    3 months
    Title
    Patient-Related Tennis Elbow Evaluation (PRTEE) functional disability
    Description
    Rates from 0 (no difficulty) to 10 (unable to do) on specific activities and usual activities. Specific activities include turning doorknob or key, carrying grocery bag or briefcase by handle, lifting full coffee cup or glass of milk to mouth, opening jars, pulling up pants, wringing out washcloths or wet towels. Usual activities include personal activities (dressing, washing), household work (cleaning, maintenance), work (job), recreational or sporting activities.
    Time Frame
    6 months
    Title
    Visual analog scale (VAS) pain with resisted wrist extension
    Description
    Rated from 0 (no pain) to 5 (extremely pain)
    Time Frame
    baseline
    Title
    Visual analog scale (VAS) pain with resisted wrist extension
    Description
    Rated from 0 (no pain) to 5 (extremely pain)
    Time Frame
    6 weeks
    Title
    Visual analog scale (VAS) pain with resisted wrist extension
    Description
    Rated from 0 (no pain) to 5 (extremely pain)
    Time Frame
    3 months
    Title
    Visual analog scale (VAS) pain with resisted wrist extension
    Description
    Rated from 0 (no pain) to 5 (extremely pain)
    Time Frame
    6 months
    Title
    Visual analog scale (VAS) pain with contraction of extensor carpi radialis brevis and extensor digitorum communis
    Description
    Rated from 0 (no pain) to 5 (extremely pain)
    Time Frame
    baseline
    Title
    Visual analog scale (VAS) pain with contraction of extensor carpi radialis brevis and extensor digitorum communis
    Description
    Rated from 0 (no pain) to 5 (extremely pain)
    Time Frame
    6 weeks
    Title
    Visual analog scale (VAS) pain with contraction of extensor carpi radialis brevis and extensor digitorum communis
    Description
    Rated from 0 (no pain) to 5 (extremely pain)
    Time Frame
    3 months
    Title
    Visual analog scale (VAS) pain with contraction of extensor carpi radialis brevis and extensor digitorum communis
    Description
    Rated from 0 (no pain) to 5 (extremely pain)
    Time Frame
    6 months
    Title
    Ultrasound tendon
    Description
    Ultrasonographic changes in tendon thickness and color Doppler activity will be recorded
    Time Frame
    baseline
    Title
    Ultrasound tendon
    Description
    Ultrasonographic changes in tendon thickness and color Doppler activity will be recorded
    Time Frame
    6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    21 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients of age >21 years old History of chronic pain on the lateral side of the elbow and pain on lateral epicondyle on direct palpation and resisted dorsiflexion of the wrist for more than 3 months Ability of patients to provide informed consent Exclusion Criteria: Previous tennis elbow surgery to affected elbow Previous corticosteroid injections to affected elbow Concurrent complementary and alternative medicine (CAM) treatments e.g. acupuncture Inflammatory diseases / infection / fracture / trauma Neck pain on ipsilateral side Chronic pain syndromes Malignancies Pregnant or lactating females Consistent use of NSAIDs within 48 hours of procedure Systemic use of corticosteroids within 2 weeks History of anemia, any blood disorders, hypothyroidism
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Kenon Chua
    Phone
    +65 6222 3322
    Email
    kenonchua@icloud.com

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    PRP Versus Saline in Lateral Epicondylitis

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