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Treatment of Knee Arthrosis With Platelet-derived Growth Factors vs. Hyaluronic Acid.

Primary Purpose

Knee Osteoarthrosis

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
intraarticular injections of platelet lysate
hyaluronic acid
Sponsored by
IRCCS Policlinico S. Matteo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthrosis focused on measuring knee arthrosis, platelet-derived growth factors

Eligibility Criteria

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

Inclusion Criteria:

  • grade II/III OA of the knee demonstrated at MRI17,18, according to Shahriaree Classification System - modified
  • no previous OA treatment with local hyaluronic acid or steroid injections
  • ife expectancy >1 year
  • no ongoing pregnancy
  • ability to understand and complete clinical and functional scales Lysholm, WOMAC, AKS, VAS
  • written consent.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Platelet-rich plasma

    hyaluronic acid

    Arm Description

    Patients in the intervention group will receive three autologous PRP plus calcium gluconate (as activator) intraarticular injections at 4-week intervals. Briefly, at the Immunohaematology and Transfusion Service, on each scheduled visit 20 ml of autologous whole blood will be sampled from each patient, 2 ml ACD-A will be added directly the syringe as anticoagulant; finally the vial will be gently centrifuged at 900rpm for 7 minutes. Platelet-rich plasma was collected. The PRP vials plus activator will be immediately shipped to the rehabilitation unit, where intraarticular injection will be performed by an experienced physiatrist.

    Patients in the control group will receive three intraarticular hyaluronic acid (20 mg/2 mL; Hyalgan, Fidia, Abano Terme, Italy) injections at the same intervals, by the same study staff.

    Outcomes

    Primary Outcome Measures

    Efficacy (as determined by improvement at MRI 6 months after the first injection) of intraarticular injections of platelet lysate
    Each knee was improvement, from baseline, by at least one degree the maximum MRI score (Shahriaree Classification System - modified) at 6 month

    Secondary Outcome Measures

    WOMAC functional scale
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    Lysholm functional scale
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    Tegner Knee functional scale
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    AKS functional scale
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    Lequesne functional scale
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    VAS for pain
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    Adverse event
    number of patients and knees with adverse event (any); anticipated potential adverse events were infection, anaphylaxis, hematoma

    Full Information

    First Posted
    October 29, 2016
    Last Updated
    November 8, 2016
    Sponsor
    IRCCS Policlinico S. Matteo
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02958761
    Brief Title
    Treatment of Knee Arthrosis With Platelet-derived Growth Factors vs. Hyaluronic Acid.
    Official Title
    Treatment of Knee Arthrosis: Platelet-derived Growth Factors vs. Hyaluronic Acid. A Phase II-III Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    August 2010 (undefined)
    Primary Completion Date
    January 2014 (Actual)
    Study Completion Date
    July 2014 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    IRCCS Policlinico S. Matteo

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Primary aim of this trial was to assess efficacy three intraarticular injections of platelet lysate when compared to hyaluronic acid. Additional objectives were to compare the treatment groups in terms of a number of functional scales and of number of adverse events.
    Detailed Description
    Intra-articular injections of hyaluronic acid are effective in improving symptoms and slow disease progression, but are not able to revert the damage mechanism and trigger cartilage healing. Growth factors included in PRP could stimulate cartilage repair, normalize synovial fluid viscoelasticity, induce a correction in tissue damage, improve articular function, control pain and ameliorate quality of life. Primary aim of this trial was to assess, among patients with grade II/III osteoarthrosis of the knee, efficacy (as determined by improvement at MRI 6 months after the first injection) of three intraarticular injections of platelet lysate when compared to hyaluronic acid. Additional objectives were to compare the treatment groups in terms of a number of functional scales (WOMAC, Lysholm, Tegner Knee, Scale, AKS, Lequesne, VAS) and of number of adverse events.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Knee Osteoarthrosis
    Keywords
    knee arthrosis, platelet-derived growth factors

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    InvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    58 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Platelet-rich plasma
    Arm Type
    Experimental
    Arm Description
    Patients in the intervention group will receive three autologous PRP plus calcium gluconate (as activator) intraarticular injections at 4-week intervals. Briefly, at the Immunohaematology and Transfusion Service, on each scheduled visit 20 ml of autologous whole blood will be sampled from each patient, 2 ml ACD-A will be added directly the syringe as anticoagulant; finally the vial will be gently centrifuged at 900rpm for 7 minutes. Platelet-rich plasma was collected. The PRP vials plus activator will be immediately shipped to the rehabilitation unit, where intraarticular injection will be performed by an experienced physiatrist.
    Arm Title
    hyaluronic acid
    Arm Type
    Active Comparator
    Arm Description
    Patients in the control group will receive three intraarticular hyaluronic acid (20 mg/2 mL; Hyalgan, Fidia, Abano Terme, Italy) injections at the same intervals, by the same study staff.
    Intervention Type
    Biological
    Intervention Name(s)
    intraarticular injections of platelet lysate
    Intervention Type
    Drug
    Intervention Name(s)
    hyaluronic acid
    Intervention Description
    intraarticular hyaluronic acid (20 mg/2 mL; Hyalgan, Fidia, Abano Terme, Italy) injections at the same intervals
    Primary Outcome Measure Information:
    Title
    Efficacy (as determined by improvement at MRI 6 months after the first injection) of intraarticular injections of platelet lysate
    Description
    Each knee was improvement, from baseline, by at least one degree the maximum MRI score (Shahriaree Classification System - modified) at 6 month
    Time Frame
    Six months after the last infiltration
    Secondary Outcome Measure Information:
    Title
    WOMAC functional scale
    Description
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    Time Frame
    At baseline (prior to treatment), at 15 days form the last injection, 6 months from the last infiltration and at 1 year
    Title
    Lysholm functional scale
    Description
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    Time Frame
    At baseline (prior to treatment), at 15 days form the last injection, 6 months from the last infiltration and at 1 year
    Title
    Tegner Knee functional scale
    Description
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    Time Frame
    At baseline (prior to treatment), at 15 days form the last injection, 6 months from the last infiltration and at 1 year
    Title
    AKS functional scale
    Description
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    Time Frame
    At baseline (prior to treatment), at 15 days form the last injection, 6 months from the last infiltration and at 1 year
    Title
    Lequesne functional scale
    Description
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    Time Frame
    At baseline (prior to treatment), at 15 days form the last injection, 6 months from the last infiltration and at 1 year
    Title
    VAS for pain
    Description
    multilevel generalized linear models (for panel-data) with interaction between time and treatment group
    Time Frame
    At baseline (prior to treatment), at 15 days form the last injection, 6 months from the last infiltration and at 1 year
    Title
    Adverse event
    Description
    number of patients and knees with adverse event (any); anticipated potential adverse events were infection, anaphylaxis, hematoma
    Time Frame
    1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: grade II/III OA of the knee demonstrated at MRI17,18, according to Shahriaree Classification System - modified no previous OA treatment with local hyaluronic acid or steroid injections ife expectancy >1 year no ongoing pregnancy ability to understand and complete clinical and functional scales Lysholm, WOMAC, AKS, VAS written consent.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Claudio Lisi, MD
    Organizational Affiliation
    IRCCS Policlinico S. Matteo
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Treatment of Knee Arthrosis With Platelet-derived Growth Factors vs. Hyaluronic Acid.

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