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Bone Marrow Aspirate in Primary Knee Osteoarthritis

Comparative analysis of Bone Marrow Aspirate versus Bone Marrow Aspirate Concentrate in Primary Knee Osteoarthritis - An Unicentric, double blinded, randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097973
Enrollment
200
Registered
2025-11-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Health Condition 1: M170- Bilateral primary osteoarthritis of knee

Interventions

Intervention1: Bone Marrow Aspirate Concentrate: Group A: Single dose of 5 ml subchondral BMAC (both tibial and femoral medial condyles) on day 0 Group B: Single dose of 5 ml intraarticular BMAC injec

Sponsors

Ashwini R
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with age between 40 to 60 years of both sex Patients OA knee with Grade II and III. Primary OA knee patients not responding to analgesics Patients who are willing to take part in the study after informed consent

Exclusion criteria

Exclusion criteria: Post traumatic knee Stiffness History of Infective joint disease Patients with a history of previous surgeries on the knee Comorbid or Pathology of ipsilateral Hip or foot joint pathology Patients with rheumatoid arthritis, inflammatory arthritis or polyarticular arthritis, and autoimmune diseases Any other defect of the ipsilateral limb like Shortening Patients with history of prior corticosteroid injection at treatment site within 3 months of duration

Design outcomes

Primary

MeasureTime frame
To assess the pain relief of BMAC versus BMA injections in primary osteoarthritis knee with VAS score at different follow-up time points. Timepoint: Day 0 At the end of 1,3,6,12,24 months

Secondary

MeasureTime frame
To evaluate the functional outcome of BMAC versus BMA injections in primary osteoarthritis knee with WOMAC and KOOSTimepoint: Day 0 At the end of 1,3,6,12,24 months ;To compare the cartilage thickness and the healing of subchondral bone lesions of BMAC and BMA in primary osteoarthritis knee via MOCARTTimepoint: Day 0 At the end of 24 months

Countries

India

Contacts

Public ContactAshwini R

Faculty of medicine- Sri Lalithambigai Medical College and Hospital

madhanjeyaraman@gmail.com8310600785

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026