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The Comparison of Efficacy and Safety of the Mesenchymal Stem Cells From Adipose and Hyaluronic Acid

Primary Purpose

Knee Osteoarthritis

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Mesenchymal Stem Cells from adipose
Hyaluronic Acid
Sponsored by
Peking University People's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Knee Osteoarthritis, adipose, mesenchymal stem cells

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • K / L score of 2-3;
  • chronic knee pain;
  • no local or systemic infection;
  • without obvious contraindication of the joint puncture from hematology and biochemical tests;
  • informed consent.

Exclusion Criteria:

  • older than 75 years old or less than 18 years old, or without full capacity for civil conduct;
  • HIV, hepatitis virus or syphilis virus infection or their serology is positive;
  • BMI index is greater than 30;
  • congenital or acquired knee deformity;
  • pregnant or lactating women;
  • tumor patients;
  • immunodeficiency patients;
  • intra-articular drug injection history within 3 months;
  • participating in other clinical trials;
  • other patients who researchers believe are not eligible for inclusion such as suffering from other concomitant diseases.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Mesenchymal Stem Cells from adipose

    hyaluronic acid

    Arm Description

    Mesenchymal Stem Cells from adipose will be injected.

    Hyaluronic acid will be injectied.

    Outcomes

    Primary Outcome Measures

    Unexplained local and systemic symptoms or death
    The severity of AE must be recorded and graded according to the CTCAE criteria, and its relationship to therapy must be assessed according to the following definition:①not related: there is evidence that the cause of adverse events is not due to intra-articular injection therapy (such as previous conditions, potential diseases, concurrent diseases); ②related: AE and intra-articular injection are time-related and it is known or suspected that intra-articular injection of drugs can cause the AE; ③it can't be assessed.

    Secondary Outcome Measures

    VAS score
    VAS score decrease 3 points or more
    WOMAC score
    two or more terms of WOMAC score have improvement.

    Full Information

    First Posted
    November 25, 2017
    Last Updated
    November 29, 2017
    Sponsor
    Peking University People's Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03357575
    Brief Title
    The Comparison of Efficacy and Safety of the Mesenchymal Stem Cells From Adipose and Hyaluronic Acid
    Official Title
    The Comparison of Efficacy and Safety of the Mesenchymal Stem Cells From Adipose and Hyaluronic Acid in the Treatment of Adult Knee Osteoarthritis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2017
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 1, 2018 (Anticipated)
    Primary Completion Date
    June 1, 2020 (Anticipated)
    Study Completion Date
    December 1, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Peking University People's Hospital

    4. Oversight

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

    5. Study Description

    Brief Summary
    The aim of this study was to evaluate the efficacy and safety of Mesenchymal Stem Cells (MSCs) from adipose anticular injection in comparison with hyaluronic acid anticular injection in the treatment of human knee osteoarthritis(OA).
    Detailed Description
    This is a single-centre, quadruple blined, randomized controlled clinical trials with a total of 14 knee osteoarthrits patients as participants, who will be randomly assigned into experiment group or compare group.Participants in experiment group will receive the treatment of MSCs from adipose anticular injection, while participants in compare group will receive hyaluronic acid. Unexplained local and systemic symptoms as well as visual analog scale pain score, WesternOntario McMasterUniversities (WOMAC) Osteoarthritis Index scorewill be assessed at baseline and 2 years after the injection.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Knee Osteoarthritis
    Keywords
    Knee Osteoarthritis, adipose, mesenchymal stem cells

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    14 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Mesenchymal Stem Cells from adipose
    Arm Type
    Experimental
    Arm Description
    Mesenchymal Stem Cells from adipose will be injected.
    Arm Title
    hyaluronic acid
    Arm Type
    Active Comparator
    Arm Description
    Hyaluronic acid will be injectied.
    Intervention Type
    Biological
    Intervention Name(s)
    Mesenchymal Stem Cells from adipose
    Intervention Description
    inject mesenchymal Stem Cells from adipose
    Intervention Type
    Biological
    Intervention Name(s)
    Hyaluronic Acid
    Intervention Description
    inject hyaluronic acid
    Primary Outcome Measure Information:
    Title
    Unexplained local and systemic symptoms or death
    Description
    The severity of AE must be recorded and graded according to the CTCAE criteria, and its relationship to therapy must be assessed according to the following definition:①not related: there is evidence that the cause of adverse events is not due to intra-articular injection therapy (such as previous conditions, potential diseases, concurrent diseases); ②related: AE and intra-articular injection are time-related and it is known or suspected that intra-articular injection of drugs can cause the AE; ③it can't be assessed.
    Time Frame
    2 years
    Secondary Outcome Measure Information:
    Title
    VAS score
    Description
    VAS score decrease 3 points or more
    Time Frame
    2 years
    Title
    WOMAC score
    Description
    two or more terms of WOMAC score have improvement.
    Time Frame
    2 years

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: K / L score of 2-3; chronic knee pain; no local or systemic infection; without obvious contraindication of the joint puncture from hematology and biochemical tests; informed consent. Exclusion Criteria: older than 75 years old or less than 18 years old, or without full capacity for civil conduct; HIV, hepatitis virus or syphilis virus infection or their serology is positive; BMI index is greater than 30; congenital or acquired knee deformity; pregnant or lactating women; tumor patients; immunodeficiency patients; intra-articular drug injection history within 3 months; participating in other clinical trials; other patients who researchers believe are not eligible for inclusion such as suffering from other concomitant diseases.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Ziyi Yang, MD
    Phone
    18810335110
    Email
    bjmuyangziyi@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ziyi Yang
    Organizational Affiliation
    arthritis clinic and research center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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