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On Real world population to evaluate clinical performance and survivorship of freedom in Total Knee system

A real world, Clinical Evaluation of Performance and survivorship of Freedom® Total Knee System in Total Knee Arthroplasty

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/11/006372
Enrollment
150
Registered
2015-11-20
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patients who have been treated with Freedom® Total Knee System

Interventions

Intervention1: Freedom Knee system: Size: Various size Product Selection: Appropriate matching of the component will occur when the articular component matched to the femoral component. Control Interv

Sponsors

Dr Avtar singh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male or female with age >= 18 years 2. The subjects who have been completed at least >= 3 years after Total Knee Replacement surgery treated with Freedom® Total Knee System by Dr. Avtar Singh and his team. 3. The subjects who are contactable, willing to participate in the survey study by signing voluntary informed consent form in accordance with regulatory guidelines.

Exclusion criteria

Exclusion criteria: 1. The subjects who have been treated with Freedom® Total Knee System but have not completed 3 years after total knee replacement surgery. 2. Subjects who are unwilling to participate in the clinical study. 3. Subjects who have more than one type of knee implant i.e. who have implant/s other than Freedom® Total Knee System. 4. Subjects suffering from rheumatoid arthritis at the time of procedure. 5. Subjects who have undergone knee replacement due to accidental injury. 6. Subjects with BMI > 30.

Design outcomes

Primary

MeasureTime frame
Maximum Range of Motion in patients who have been completed at least � 3 years after Total Knee Replacement surgery.Timepoint: The subjects who have been completed at least � 3 years after Total Knee Replacement surgery treated with Freedom® Total Knee System

Secondary

MeasureTime frame
1. To determine Clinical and Social Quality of life as per American Knee Society Score (AKSS). 2. To evaluate pain relief as per Modified WOMAC Pain and Stiffness Score.Timepoint: The subjects who have been completed at least � 3 years after Total Knee Replacement surgery treated with Freedom® Total Knee System

Countries

India

Contacts

Public ContactDr Avtar Singh

Amandeep Hospital

ah.edu@amandeephospital.org9876150258

Outcome results

None listed

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