PIKASO: Preventing Injured Knees From osteoArthritis: Severity Outcomes

Sponsor
Brigham and Women's Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06096259
Collaborator
Arthritis Foundation (Other)
512
9
2
72
56.9
0.8

Study Details

Study Description

Brief Summary

This study is being done to find out if metformin is effective at reducing pain by delaying the onset of post-traumatic osteoarthritis (PTOA) after anterior cruciate ligament (ACL) reconstruction. This research study will compare metformin to placebo. The placebo tablet looks exactly like metformin, but contains no metformin. Placebos are used in research studies to see if the results are due to the study drug or due to other reasons.

Metformin is approved by the U.S. Food and Drug Administration (FDA) to treat type II diabetes. Notably, it also has anti-inflammatory effects, suggesting it could benefit people who have an ACL injury and are undergoing ACL reconstruction.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Osteoarthritis (OA) is among the most prevalent chronic, disabling conditions, occurring in over 32 million persons in the US. Worldwide, an estimated 240 million persons have symptomatic, activity-limiting OA. OA cases arising from injury are referred to as post-traumatic OA (PTOA). Approximately 12% of cases of lower extremity symptomatic OA are PTOA, often the result of injuries such as anterior cruciate ligament (ACL) rupture or ankle fracture. Four million Americans have PTOA. On average, patients with PTOA develop knee OA 10.4 years earlier than those with primary knee OA. Similarly, individuals with PTOA of the hip and ankle develop OA 9.0 and 14.0 years, respectively, earlier than their primary OA counterparts. Sustaining ACL injury early in adulthood leads to greater lifetime risk as well as earlier onset of knee OA and need for total knee replacement (TKR). The earlier age of onset means that PTOA is often a disorder of working persons, compromising productivity and quality of life. The indirect cost burden of PTOA is estimated to be ~$4.4 billion annually, because individuals are typically affected in their most productive years of employment.

Anterior cruciate ligament (ACL) injury is the most common sports-related knee injury, and many patients who wish to return to sporting activities that involve cutting and pivoting will choose to undergo ACL reconstruction (ACLR). Each year, more than 120,000 ACL reconstructions are performed in the US alone. Even though ACLR can allow people to return to sporting activities with a stable knee, there is still an increased risk of PTOA after the ACL injury and subsequent reconstruction. Studies have demonstrated that around 50% of patients who undergo ACL reconstruction develop OA within 10-15 years. Given the large number of ACL injuries and subsequent reconstructions that occur annually, and the strong association between ACL tear/reconstruction and PTOA, developing treatment strategies to delay or prevent PTOA and promote long-term health after ACLR is critical to maintaining the well-being of young, active populations. This study proposes to address these issues by testing the efficacy of metformin, a commonly used and safe drug with promising pre-clinical and clinical evidence of PTOA prevention, in younger adults undergoing ACL reconstruction.

PIKASO is a multicenter, double-blind (participants, treating clinicians, and assessors), placebo-controlled, randomized study to establish the efficacy of metformin at delaying the onset of post-traumatic osteoarthritis (PTOA) after anterior cruciate ligament reconstruction. Subjects will be randomized in a 1:1 ratio. Each subject will complete standard-of-care postoperative physical therapy in both arms. The two primary outcomes will be KOOS pain (assessed at 12 and 24 months postoperatively and averaged) and modified MOAKS (MRI Osteoarthritis Knee Score) cartilage score at 24 months postoperatively.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
512 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Preventing Injured Knees From osteoArthritis: Severity Outcomes (PIKASO)
Anticipated Study Start Date :
Dec 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2028
Anticipated Study Completion Date :
Dec 1, 2029

Arms and Interventions

Arm Intervention/Treatment
Experimental: Metformin

3x500mg metformin HCl extended-release tablets taken orally once a day for 1 year

Drug: Metformin
Metformin is an oral anti-hyperglycemic agent widely used as first-line treatment for type II diabetes to improve glycemic control. It is the fourth most commonly prescribed drug in the United States. Participants will receive commercially available extended-release metformin 500mg tablets manufactured by Granules India Limited, Hyderabad, India and then sourced, packaged, and labeled for the study by Sharp Labs. The study will follow standard dosing procedures for extended-release metformin. Participants will begin by taking 1x500 mg pill once a day, and then the dose will be increased in 500 mg/day increments weekly as tolerated, up to a maximum dose of 1500 mg daily.
Other Names:
  • Glumetza
  • Fortamet
  • Glucophage XR
  • Placebo Comparator: Placebo

    3x metformin placebo tablets matching metformin extended-release taken orally once a day for 1 year

    Drug: Placebo
    The study will use matching placebo tablets that are almost indistinguishable from the 500 mg metformin ER tablets. Participants will begin by taking 1x500 mg pill once a day, and then the dose will be increased in 500 mg/day increments weekly as tolerated, up to a maximum dose of 1500 mg daily.

    Outcome Measures

    Primary Outcome Measures

    1. KOOS Pain Score [Average of 12 and 24 months]

      To determine whether metformin leads to reduced pain as measured by the KOOS pain subscale compared to placebo between 12 and 24 months postoperatively. Knee Injury and Osteoarthritis Outcome Score (KOOS) is a questionnaire designed to assess short and long-term patient-relevant outcomes following knee injury. The KOOS pain subscale contains 9 items and is scored on a 0-100 scale, 100 being best.

    2. Modified MOAKS Cartilage Score [24 months]

      To determine whether metformin leads to reduced structural degeneration at 24 months postoperatively compared to placebo. The MOAKS score (MRI Osteoarthritis Knee Score) is a semi-quantitative whole joint assessment of knee osteoarthritis with very good to excellent reliability used to score knee osteoarthritis. In MOAKS the knee is divided into 14 articular subregions for scoring articular cartilage and bone marrow lesions (BMLs) and in addition the subspinous region is added for BML scoring. For each region, the following features are assessed independently: bone marrow lesions and cysts (score: 0-3, 3 worst) articular cartilage loss (score: 0-3, 3 worst) osteophytes (score: 0-3, 3 worst) synovitis and effusion (score: 0-3, 3 worst) meniscus extrusion and morphology (score: 0-3, 3 worst) ligaments/tendon (0/1, 0=normal, 1=abnormal) periarticular features (0/1, 0=absent, 1=present)

    Secondary Outcome Measures

    1. KOOS Pain [baseline, 3 months, 6 months, 9 months, 12 months, 18 months, 24 months]

      Assessed via questionnaire. Knee Injury and Osteoarthritis Outcome Score (KOOS) is a questionnaire designed to assess short and long-term patient-relevant outcomes following knee injury. The KOOS is self-administered and includes 42 items across 5 subscales: pain, symptoms, ADLs, sports/recreation, and quality of life. KOOS is scored on a 0-100 scale, 100 being best. The pain subscale contains 9 items.

    2. KOOS Symptoms [baseline, 3 months, 6 months, 9 months, 12 months, 18 months, 24 months]

      Assessed via questionnaire. Knee Injury and Osteoarthritis Outcome Score (KOOS) is a questionnaire designed to assess short and long-term patient-relevant outcomes following knee injury. The KOOS is self-administered and includes 42 items across 5 subscales: pain, symptoms, ADLs, sports/recreation, and quality of life. KOOS is scored on a 0-100 scale, 100 being best. The symptoms subscale contains 7 items.

    3. KOOS Activities of Daily Living [baseline, 3 months, 6 months, 9 months, 12 months, 18 months, 24 months]

      Assessed via questionnaire. Knee Injury and Osteoarthritis Outcome Score (KOOS) is a questionnaire designed to assess short and long-term patient-relevant outcomes following knee injury. The KOOS is self-administered and includes 42 items across 5 subscales: pain, symptoms, ADLs, sports/recreation, and quality of life. KOOS is scored on a 0-100 scale, 100 being best. The ADL subscale contains 17 items.

    4. KOOS Sport and Recreation Function [baseline, 3 months, 6 months, 9 months, 12 months, 18 months, 24 months]

      Assessed via questionnaire. Knee Injury and Osteoarthritis Outcome Score (KOOS) is a questionnaire designed to assess short and long-term patient-relevant outcomes following knee injury. The KOOS is self-administered and includes 42 items across 5 subscales: pain, symptoms, ADLs, sports/recreation, and quality of life. KOOS is scored on a 0-100 scale, 100 being best. The sports and recreation subscale contains five items.

    5. KOOS Quality of Life [baseline, 3 months, 6 months, 9 months, 12 months, 18 months, 24 months]

      Assessed via questionnaire. Knee Injury and Osteoarthritis Outcome Score (KOOS) is a questionnaire designed to assess short and long-term patient-relevant outcomes following knee injury. The KOOS is self-administered and includes 42 items across 5 subscales: pain, symptoms, ADLs, sports/recreation, and quality of life. KOOS is scored on a 0-100 scale, 100 being best. The quality of life subscale contains four items.

    6. Marx Activity Rating Scale [baseline, 12 months, 24 months]

      Assessed via questionnaire The Marx Scale consists of four questions concerning running, cutting, deceleration, and pivoting. The patient is asked to report on the frequency with which they performed the activity in their healthiest state within the past year. It is most often used in physically active adults aged 18-50 with knee problems.

    7. Work Productivity and Activity Impairment (WPAI) [baseline, 3 months, 6 months, 9 months, 12 months, 18 months, 24 months]

      Assessed via questionnaire The Work Productivity and Activity Impairment (WPAI) questionnaire is a 6-item instrument to measure impairments in both paid work and unpaid work. It measures impairments in paid work and other activity because of health problems during the past seven days.

    8. EuroQoL Score (EQ-5D-5L) [baseline, 3 months, 6 months, 9 months, 12 months, 18 months, 24 months]

      Assessed via questionnaire The 5-level EQ-5D version (EQ-5D-5L) is a quality of life measure that includes two components: the EQ-5D descriptive system and the EQ visual analogue scale (EQ VAS). The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The scores for the five dimensions can be combined into a 5-digit number that describes the patient's health state (5-25, 25 worst). The EQ VAS records the patient's self-rated health on a visual analogue scale (0-100, 100 best).

    9. Tampa Scale of Kinesiophobia Score [baseline, 3 months, 6 months, 9 months, 12 months, 18 months, 24 months]

      Assessed via questionnaire The Tampa Scale of Kinesiophobia is a 17-item questionnaire with a 4-point Likert scale to assess one's fear of movement or reinjury. Two subscales make up the scale: Avoiding physical exertion because of fear of reinjury or worsening of pain (Questions 1, 2, 7, 9, 10, 11, 12) Somatic Focus - the idea that there are underlying, major medical issues involved (Questions 3, 4, 5, 6, 8) Individual item scores range from 1-4 (4 worst), with the negatively worded items (4, 8, 12, 16) having a reverse scoring (4-1, 1 worst). The 17 item TSK total scores range from 17 to 68 where the lowest 17 means no kinesiophobia, and the higher scores indicate an increasing degree of kinesiophobia. Scores above 37 are generally considered to indicate kinesiophobia.

    10. MHI-5 Score [baseline, 3 months, 6 months, 9 months, 12 months, 18 months, 24 months]

      Assessed via questionnaire The Mental Health Inventory-5 (MHI-5) is a brief, valid, and reliable international instrument for assessing mental health status in adults. The MHI-5 has 5 items and is scored on a scale from 0-100, where 100 indicates optimal mental health.

    11. Joint Space Narrowing Over Time [baseline, 12 months, 24 months]

      Joint space narrowing will be measured in mm and assessed via X-Ray and MRI. Greater joint space narrowing indicates more severe structural osteoarthritis.

    12. Cartilage composition assessed with T1rho, T2 [baseline, 12 months, 24 months]

      Assessed via compositional MRI with T1rho and T2 weighted sequences, which are being investigated for their usefulness in musculoskeletal imaging, particularly for examining cartilage.

    13. Severity of Synovitis on Contrast MRI [baseline, 12 months]

      Assessed via optional contrast MRI. Dynamic contrast enhanced MR images will be analyzed to quantify variables including maximum enhancement, number of enhanced voxels, and derived variables (e.g. maximum enhancement times number of enhanced voxels) for evaluating severity of synovitis.

    14. Knee Range of Motion [12 and 24 months]

      Assessed via physical examination with a goniometer

    15. 3D Gait Biomechanics [12 and 24 months]

      Walking gait will be evaluated using a motion capture system as participants walk at a self-selected speed

    16. Isokinetic knee flexion/extension strength at 60ยบ/sec [12 and 24 months]

      Assessed using an isokinetic dynamometer

    17. 10m Habitual Walking Speed [12 and 24 months]

      The time to walk 10 m will be recorded

    18. Single Leg Hop Test [12 and 24 months]

      The maximum distance will be recorded

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Age 25-45 or Age 18-24 with preoperative KOOS Pain <80 (0-100, 100 best) recorded at least 14 days after the day of ACL injury

    2. ACL tear documented on MRI within 6 months prior to screening

    3. Plan to undergo ACL reconstruction

    Exclusion Criteria:
    1. Inflammatory arthritis

    2. Pregnancy and/or lactation, or plans to become pregnant in the next 12 months

    3. Known contraindication to metformin

    4. Current use of metformin or topiramate

    5. Type I diabetes mellitus or diabetic ketoacidosis

    6. Heavy alcohol consumption and/or known hepatic disease

    7. Acute or chronic renal insufficiency

    8. History of ACLR on either knee

    9. Applying for or receiving Workers' Compensation for their knee injury

    10. Joint space narrowing AND definite osteophyte(s) on weightbearing radiograph on index knee

    11. Tibial plateau fracture on index knee

    12. Concomitant avulsion fracture of index knee that will be treated surgically

    13. Concomitant posterior cruciate ligament, medial collateral ligament, or lateral collateral ligament injury on index knee requiring surgical repair/reconstruction

    14. Contraindication to MRI

    15. Unable to speak and understand English

    16. Diagnosis of cognitive impairment or otherwise unable to provide informed consent

    17. Insufficient time for recruitment and drug titration: Surgery scheduled for <14 days from the time of screening

    18. Presence of a condition or abnormality that in the opinion of the surgeon investigator would compromise the safety of the patient or the quality of the data

    19. Plan for allograft at time of consent

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Emory University Atlanta Georgia United States 30322
    2 University of Iowa Hospitals and Clinics Iowa City Iowa United States 52242
    3 University of Kentucky Lexington Kentucky United States 40504
    4 Brigham and Women's Hospital Boston Massachusetts United States 02115
    5 University of Nebraska Medical Center Omaha Nebraska United States 68198
    6 Hospital for Special Surgery New York New York United States 10021
    7 The University of North Carolina at Chapel Hill Chapel Hill North Carolina United States 25599
    8 Cleveland Clinic Cleveland Ohio United States 44195
    9 The Ohio State University Columbus Ohio United States 43210

    Sponsors and Collaborators

    • Brigham and Women's Hospital
    • Arthritis Foundation

    Investigators

    • Principal Investigator: Morgan H Jones, MD, MPH, Brigham and Women's Hospital
    • Principal Investigator: Cale A Jacobs, PhD, Brigham and Women's Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Morgan H. Jones, MD, MPH, Assistant Professor of Orthopedic Surgery, Brigham and Women's Hospital
    ClinicalTrials.gov Identifier:
    NCT06096259
    Other Study ID Numbers:
    • 2023P002573
    First Posted:
    Oct 23, 2023
    Last Update Posted:
    Oct 23, 2023
    Last Verified:
    Oct 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 23, 2023