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Observing how knee joint arthritis progresses using range of joint movements and MRI data: A Longterm comparative study

Assessing the progression of Knee Joint Osteoarthritis using Arthro-kinematic and Finite Element Analysis: A Prospective Cohort study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/081105
Enrollment
55
Registered
2025-02-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: Anthropometric, biomechanical and finite element analysis of knee joint: The patients will be selected using eligibility criteria and will be divided into two groups: the intervention/s

Sponsors

All India Institute of Medical Sciences AIIMS Rajkot
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age 35 years and above. 2. Patient with degenerative changes in knee with any deviation from the normal mechanical axis.

Exclusion criteria

Exclusion criteria: 1. Patients under 35 years. 2. Patients with any contraindication for MRI like electronic device, metallic implants, etc. 3. Patients with claustrophobia. 4. Neurological disorders, systemic disorders, muscular dystrophy, metabolic bone diseases affecting bone metabolism. 5. Soft tissue, or bone swelling causing knee misalignment. 6. Axial skeleton deformities. 7. Conditions requiring surgery. 8. Already operated cases for knee joint osteoarthritis. 9. Gross deformity in proximal (hip) and distal (ankle joint and foot) segments. 10. BMI above morbid obesity.

Design outcomes

Primary

MeasureTime frame
The patients will be selected using eligibility criteria and provide written consent. Demographics and medical history will be recorded via a patient information sheet. They will be divided into two groups: the study group, receiving customized orthotics after correction of the knee joint mechanical axis, and the control group, receiving conventional management (e.g., physiotherapy, knee belt). Both groups will be followed up at 3-month intervals. At baselines: A.MRI will be done of the knee joint affected side. B. Anthropometric analysis of knee joint variables will be conducted as follows using RadiANT DICOM Viewer software: C. Knee joint biomechanical findings (Range of motion) 1.Flexion at knee joint (Active/passive) 2.Extension at knee joint (Active/passive) 3.Internal rotation (active/passive) 4.External rotation (active/passive) Timepoint: Both groups will be followed up at 3-month intervals. MRI will be performed at the baseline and will be done at 9 and 18 months, whereas arthro-kinematic analysis shall be done at 3, 6, 9, 12, 15 and 18 months.

Secondary

MeasureTime frame
Finite element analysis of the knee joint (side) will be done using the sift copies of the MRI scans using the following parameters: 1 Contact area (mm3) 2 Contact pressure (MPa) Mean/Peak 3 Pore pressure (MPa) Mean/Peak 4 Tensile stress% (Mean/Peak) 5 Tensile strain% (Mean/Peak) 6 Translation of medial femoral condyle(mm) 7 Translation of lateral femoral condyle (mm) 8 Mechanical axis of hip joint 9 Femoro-tibial (Knee joint) mechanical axis 10 Medial collateral ligaments 11 Lateral collateral ligaments Timepoint: Both groups will be followed up at 3-month intervals. MRI will be performed at the baseline and will be done at 9 and 18 months, whereas arthro-kinematic analysis shall be done at 3, 6, 9, 12, 15 and 18 months. Finite element analysis will be done at baseline, 9 months and 18 months stage in the follow up.

Countries

India

Contacts

Public ContactDr Sundip Charmode

All-India Institute of Medical Sciences Rajkot

sundip.charmode@yahoo.com09633239685

Outcome results

None listed

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