Intra Articular Injection of Microfat and PRP in Knee Osteoarthritis

Knee Osteoarthritis Clinical Trial

— MICROPREP  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04352075
• Other study ID #: 2016-004755-75
• Secondary ID: 2016-004755-75
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: November 15, 2018
• Est. completion date: March 1, 2020

Study information

• Verified date: April 2020
• Source: Clinique Juge
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: March 1, 2020
• Est. primary completion date: August 1, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Knee Osteoarthritis
• Osteoarthritis
• Osteoarthritis, Knee

Intervention

Drug:
• Autologous biologic drug of innovative therapy /cell therapy drug
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

Locations

Country	Name	City	State
France	Louis	Marseille

Sponsors (1)

Lead Sponsor	Collaborator
Clinique Juge

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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.	Baseline and 3 months post injection
Secondary	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.	Baseline and 3 and 6 months post injection
Secondary	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)	Baseline and 1 and 3 and 6 months post injection
Secondary	Responding patients	The proportion of patients not responding to treatment.	Baseline and 3 and 6 months post injection
Secondary	Biologic parameters / clinical efficacity	The correlation between clinical efficacy and dose of PRP administered and dose of growth factors administered.	Baseline and 3 and 6 months post injection
Secondary	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)	Baseline and 1 and 3 and 6 months post injection