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Clinical Trial of Autologous Adipose Tissue-Derived Mesenchymal Progenitor Cells (MPCs) Therapy for Knee Osteoarthritis

A PhaseⅡb, Randomized, Double-blinded, Clinical Trial of Autologous Adipose Tissue-Derived Mesenchymal Progenitor Cells Therapy for Knee Osteoarthritis

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02162693
Enrollment
53
Registered
2014-06-13
Start date
2013-11-30
Completion date
2016-11-30
Last updated
2017-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis

Brief summary

Current medication treatments for KOA aim to relieve inflammation and pain, but they do little to delay or reverse the disease progression and most medications have obvious side effects. When the conservative treatments are useless to patients and joint deformities and joint disfunction, the patients may require surgery. Although surgery of the joints can relieve the pain temporarily, long-term effect (over 10 years) is hard to achieve.

Detailed description

Human adipose-derived mesenchymal progenitor cells (haMPCs) are obtained through a series of procedures: firstly, the fresh adipose tissue is digested with collagenase, filtered, centrifuged and then discard mature adipose cells to obtain adipose tissue-derived nuclear cells also called stromal vascular fraction cells (SVFs). In the end, haMPCs are prepared after being purified andamplified to P2-P5. When induced by specific factors, haMPCs have a potential for multilineage differentiation towards bone, cartilage and fat tissue both in vivo and in vitro. The haMPCs can secrete a number of soluble mediators to stimulate the proliferation of endogenous progenitor cells, to act as nutrients, to be immunosuppressive, to be anti-inflammatory, to prevent fibrosis and promote angiogenesis. The cytokines secreted by haMPCs play a synergic role in restoring the dynamic balance of synthesis and decompositon of cartilage tissue, and finally to repair the impaired cartilage.

Interventions

Administrated for intra-articular injection

BIOLOGICALSodium Hyaluronate

Sponsors

RenJi Hospital
CollaboratorOTHER
General Hospital of Chinese Armed Police Force
CollaboratorUNKNOWN
Shanghai AbelZeta Ltd.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. The subject is between 18-70 years of age, regardless of gender 2. The subject has a Kellgren-Lawrence grading, as determined by American College of Rheumatology (ACR) criteria for osteoarthritis of the knee, below grade 4 3. The subject or the subject's legally acceptable representative must be willing to participate in the trial, to receive cell therapy and to provide signed and dated informed consent forms

Exclusion criteria

1. The subject has an allergic history or is of an allergic constitution 2. The subject has uncontrolled or hard-to-control diseases of heart, liver, kidney or lung 3. The subject has uncontrolled or hard-to-control diseases of cardiovascular or endocrine system 4. The subject has severe infectious diseases or a malignant tumour 5. The subject has coagulation disorders 6. The subject has a BMI of over 30 7. The subject has used traditional Chinese medicine containing anti-inflammatory agents in the 2 weeks preceding the trial 8. The subject has received other intra-articular injections in the 2 months preceding the trial 9. The subject has complications or diseases of: systemic or rheumatoid arthritis, Chondrocalcinosis articular, Hemochromatosis,inflammatory arthropathy,avascular necrosis of femoral head,Paget's disease,hemophilic arthropathy,infectional arthritis,Charcot's disease,villonodular synovitis or synovial chondromatosis 10. The subject tests positive for: HIV, hepatitis virus, syphilis or other infectious diseases 11. The subject has a history of alcoholism, drug abuse, or mental illness 12. The subject has participated in any other clinical trial in the 3 months prior to this trial 13. The subject is pregnant, lactating or is planning to conceive within the next 6 months 14. The subject has any other unsuitable or adverse condition to be determined by the investigator

Design outcomes

Primary

MeasureTime frame
WOMAC Score(The Western Ontario and McMaster Universities Osteoarthritis Index)12 months

Secondary

MeasureTime frame
Recording of Adverse Events and Serious Adverse Events12 months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026