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Intra Articular Injection of Microfat and PRP in Knee Osteoarthritis (MICROPREP)

Primary Purpose

Knee Osteoarthritis

Status
Completed
Phase
Phase 1
Locations
France
Study Type
Interventional
Intervention
Autologous biologic drug of innovative therapy /cell therapy drug
Sponsored by
Clinique Juge
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis focused on measuring knee, osteoarthritis, microfat, platelet rich plasma

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Males and females between 20 to 65 years of age
  • Symptomatic knee osteoarthritis , ICRS grade 2, 3 ou 4 with VAS > 4 and failure of medical treatment for at least one year
  • BMI between 20 to 30
  • Written informed consent, signed by patient or legal representative
  • HB > 10g/dl
  • Negative pregnancy test
  • Social security affiliated

Exclusion Criteria:

  • IRM contre-indications: ocular loose bodies, pace maker, neurostimulateur, cochlear implant, vascular clips, mettalic cardiac valve
  • BMI < 20
  • Thrombocytopenia < 150 G/L
  • Thrombocytosis > 450 G/L
  • Thrombopathy
  • TP < 70%
  • TCA patient / witness rapport > 1,20
  • Anaemia: HB < 10g/dl
  • Positive serology VIH1 and 2, Agp24, Ac HCV, Ag HbS, AcHbc, Ac HTLV I and II, TPHA
  • Treatment by platelet inhibiting agent, aspirin, anti vitamin K completed more than 2 weeks before inclusion
  • Chronic treatment by corticosteroid per os or treatment completed more than 2 weeks before inclusion
  • Intra articular knee injection of corticosteroid more than 8 weeks before inclusion
  • Intra articular knee injection of hyaluronic acid more than 8 weeks before inclusion
  • NSAI treatment completed more than 2 weeks before inclusion
  • Fever or recent disease
  • Auto immune disease
  • Inflammatory Arthritis
  • Immune deficit
  • Infectious disease
  • Malignant tumor being treated or history of malignant tumor

Sites / Locations

  • Louis

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Microfat + PRP 3M platelets

Microfat + PRP 1M platelets

Microfat

Arm Description

microfat (5 ml) associated with PRP with a dose of 3 billions of platelets (5 ml)

microfat (5 ml) associated with PRP with a dose of 1 billion of platelets (5 ml)

microfat (5 ml) and saline solution (5 ml)

Outcomes

Primary Outcome Measures

Cartilage relaxation time on MRI T2-mapping at 3 months
The primary objective of this study is to demonstrate the efficacy of intra-articular injection of autologous microfat associated with a standardized preparation of autologous PRP, by changes in the cartilage relaxation time on MRI T2-mapping at 3 months.

Secondary Outcome Measures

Improved of chondral lesion on MRI
Improved chondral lesions at 3 months and 6 months on specific MRI cartilage sequences (DP FATSAT Axial, Axial T1, T2 mapping): quantitative morphological sequences resolution and qualitative structural sequences.
Pain
The evolution of pain with the visual analogic scale compared to the initial state (scores at baseline) and the evolution of pain (VAS score) at 1, 3 and 6 months post-injection. Scale from 0 (no pain) to 10 (maximal pain)
Responding patients
The proportion of patients not responding to treatment.
Biologic parameters / clinical efficacity
The correlation between clinical efficacy and dose of PRP administered and dose of growth factors administered.
WOMAC
The evolution of the functional impact of knee osteoarthritis with the Western Ontario and McMaster University Osteoarthritis score at 1, 3 and 6 months post-injection. Score from 0 to 96 (the worst)

Full Information

First Posted
April 15, 2020
Last Updated
April 17, 2020
Sponsor
Clinique Juge
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1. Study Identification

Unique Protocol Identification Number
NCT04352075
Brief Title
Intra Articular Injection of Microfat and PRP in Knee Osteoarthritis
Acronym
MICROPREP
Official Title
Intra Articular Injection of Autologous Microfat and Platelet-rich Plasma in the Treatment of Knee Osteoarthritis: a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
November 15, 2018 (Actual)
Primary Completion Date
August 1, 2019 (Actual)
Study Completion Date
March 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Clinique Juge

4. Oversight

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

5. Study Description

Brief Summary
The hypothesis of this project is that the injection of an innovative treatment (microfat and dose of autologous PRP) allows to delay knee arthroplasty in patients with knee OA resistant to medical treatment.
Detailed Description
Osteoarthritis is the most common joint disease in the world and one of the most common causes of pain and functional disability. The incidence of cartilage pathology has grown due to the ageing population, and the increase in sports participation and its associated trauma. The treatment of these cartilage damage is limited and remains a major public health issue. The aim of the medical treatment and intra articular injections consists in reducing pain and improving the knee function in order to limit the sport, professional and social negative impact in the youngest patients. Nevertheless their efficacy remain non predictable in patients. The arthroplasty will be proposed in the final intention. Insofar arthroplasty is a surgical procedure 1 / which presents a potential infectious risk associated with its invasive nature, 2 / it requires iterative revision surgery, especially in young patients given the limited lifetime of the implants and 3 / whose complete postoperative recovery take several months, it seems justified to continue studies to validate effective alternative treatments to delay the use of joint replacements. Recently, the emergence of biotherapy in orthopedics has developed the use of intra-articular injections of platelet-rich plasma (PRP). Their use has increased substantially and is based on the demonstration that platelet-rich plasma concentrate growth factors, can stimulate cartilage regeneration in vitro and in vivo preclinical models. In humans, recent data from the literature show that these autologous products are very well tolerated. Their scientific evaluation remains difficult in that 1 / indications and surgical procedures are not harmonized 2 / manufacturing processes PRP are not standardized 3 / quantitative and qualitative composition of PRP is rarely documented. PRP administration procedures can be optimized: indeed in that, it is a liquid preparation (platelet suspension), its administration in a interface tissue allows to limit its spread and potentiate its trophic effect on the injured cartilage site. Adipose tissue is the most relevant interface tissue given, because it's a tissue rich in stem cells with full therapeutic potential and is easily accessible by subcutaneous minimally invasive procedure. Thus, autologous microfat (fat removed under local anesthesia by manual liposuction using fine cannulas specific) administered in the synovial capsule, could play the matrix to receive the injection of PRP. The hypothesis of this project is that the standardized injection of an innovative treatment (microfat and dose of autologous PRP) allows to delay knee arthroplasty in patients with knee OA resistant to medical treatment. This treatment, minimally invasive and with economically reasonable cost, would provide a new treatment for second intention. In terms medicoeconomic if this treatment is effective over a period of several years, even in cases where it is necessary to do it one or two times, it would significantly reduce the financial and societal impact of joint replacements.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
knee, osteoarthritis, microfat, platelet rich plasma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Prospective, monocentric randomised, double blind
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Microfat + PRP 3M platelets
Arm Type
Experimental
Arm Description
microfat (5 ml) associated with PRP with a dose of 3 billions of platelets (5 ml)
Arm Title
Microfat + PRP 1M platelets
Arm Type
Experimental
Arm Description
microfat (5 ml) associated with PRP with a dose of 1 billion of platelets (5 ml)
Arm Title
Microfat
Arm Type
Experimental
Arm Description
microfat (5 ml) and saline solution (5 ml)
Intervention Type
Drug
Intervention Name(s)
Autologous biologic drug of innovative therapy /cell therapy drug
Intervention Description
Articular knee injection of microfat associated with a dose of 3 billions of platelets or associated with a dose of 1 billion of platelets or with saline solution
Primary Outcome Measure Information:
Title
Cartilage relaxation time on MRI T2-mapping at 3 months
Description
The primary objective of this study is to demonstrate the efficacy of intra-articular injection of autologous microfat associated with a standardized preparation of autologous PRP, by changes in the cartilage relaxation time on MRI T2-mapping at 3 months.
Time Frame
Baseline and 3 months post injection
Secondary Outcome Measure Information:
Title
Improved of chondral lesion on MRI
Description
Improved chondral lesions at 3 months and 6 months on specific MRI cartilage sequences (DP FATSAT Axial, Axial T1, T2 mapping): quantitative morphological sequences resolution and qualitative structural sequences.
Time Frame
Baseline and 3 and 6 months post injection
Title
Pain
Description
The evolution of pain with the visual analogic scale compared to the initial state (scores at baseline) and the evolution of pain (VAS score) at 1, 3 and 6 months post-injection. Scale from 0 (no pain) to 10 (maximal pain)
Time Frame
Baseline and 1 and 3 and 6 months post injection
Title
Responding patients
Description
The proportion of patients not responding to treatment.
Time Frame
Baseline and 3 and 6 months post injection
Title
Biologic parameters / clinical efficacity
Description
The correlation between clinical efficacy and dose of PRP administered and dose of growth factors administered.
Time Frame
Baseline and 3 and 6 months post injection
Title
WOMAC
Description
The evolution of the functional impact of knee osteoarthritis with the Western Ontario and McMaster University Osteoarthritis score at 1, 3 and 6 months post-injection. Score from 0 to 96 (the worst)
Time Frame
Baseline and 1 and 3 and 6 months post injection

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males and females between 20 to 65 years of age Symptomatic knee osteoarthritis , ICRS grade 2, 3 ou 4 with VAS > 4 and failure of medical treatment for at least one year BMI between 20 to 30 Written informed consent, signed by patient or legal representative HB > 10g/dl Negative pregnancy test Social security affiliated Exclusion Criteria: IRM contre-indications: ocular loose bodies, pace maker, neurostimulateur, cochlear implant, vascular clips, mettalic cardiac valve BMI < 20 Thrombocytopenia < 150 G/L Thrombocytosis > 450 G/L Thrombopathy TP < 70% TCA patient / witness rapport > 1,20 Anaemia: HB < 10g/dl Positive serology VIH1 and 2, Agp24, Ac HCV, Ag HbS, AcHbc, Ac HTLV I and II, TPHA Treatment by platelet inhibiting agent, aspirin, anti vitamin K completed more than 2 weeks before inclusion Chronic treatment by corticosteroid per os or treatment completed more than 2 weeks before inclusion Intra articular knee injection of corticosteroid more than 8 weeks before inclusion Intra articular knee injection of hyaluronic acid more than 8 weeks before inclusion NSAI treatment completed more than 2 weeks before inclusion Fever or recent disease Auto immune disease Inflammatory Arthritis Immune deficit Infectious disease Malignant tumor being treated or history of malignant tumor
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marie Laure Louis, MD
Organizational Affiliation
ICOS Corporation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Louis
City
Marseille
ZIP/Postal Code
13008
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Publication
Citations:
PubMed Identifier
33887408
Citation
Louis ML, Dumonceau RG, Jouve E, Cohen M, Djouri R, Richardet N, Jourdan E, Giraudo L, Dumoulin C, Grimaud F, George FD, Veran J, Sabatier F, Magalon J. Intra-Articular Injection of Autologous Microfat and Platelet-Rich Plasma in the Treatment of Knee Osteoarthritis: A Double-Blind Randomized Comparative Study. Arthroscopy. 2021 Oct;37(10):3125-3137.e3. doi: 10.1016/j.arthro.2021.03.074. Epub 2021 Apr 20.
Results Reference
derived

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Intra Articular Injection of Microfat and PRP in Knee Osteoarthritis

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