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Clinical Trials/NCT04352075
NCT04352075
Completed
Phase 1

Intra Articular Injection of Autologous Microfat and Platelet-rich Plasma in the Treatment of Knee Osteoarthritis: a Pilot Study

Clinique Juge1 site in 1 country30 target enrollmentNovember 15, 2018

Overview

Phase
Phase 1
Intervention
Autologous biologic drug of innovative therapy /cell therapy drug
Conditions
Knee Osteoarthritis
Sponsor
Clinique Juge
Enrollment
30
Locations
1
Primary Endpoint
Cartilage relaxation time on MRI T2-mapping at 3 months
Status
Completed
Last Updated
6 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
November 15, 2018
End Date
March 1, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Clinique Juge
Responsible Party
Principal Investigator
Principal Investigator

Marie-Laure LOUIS

Principal investigator

Clinique Juge

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

Arms & Interventions

Microfat + PRP 3M platelets

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

Intervention: Autologous biologic drug of innovative therapy /cell therapy drug

Microfat + PRP 1M platelets

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

Intervention: Autologous biologic drug of innovative therapy /cell therapy drug

Microfat

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

Intervention: Autologous biologic drug of innovative therapy /cell therapy drug

Outcomes

Primary Outcomes

Cartilage relaxation time on MRI T2-mapping at 3 months

Time Frame: Baseline and 3 months post injection

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 Outcomes

  • Improved of chondral lesion on MRI(Baseline and 3 and 6 months post injection)
  • Responding patients(Baseline and 3 and 6 months post injection)
  • Biologic parameters / clinical efficacity(Baseline and 3 and 6 months post injection)
  • Pain(Baseline and 1 and 3 and 6 months post injection)
  • WOMAC(Baseline and 1 and 3 and 6 months post injection)

Study Sites (1)

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