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TO COMPARE OUTCOMES AFTER TOTAL KNEE ARTHROPLASTY USING ULTRACONGRUENT VERSUS CRUCIATE RETAINING BEARING DESIGN TECHNIQUES

A RANDOMISED CONTROL TRIAL TO COMPARE CLINICAL, RADIOLOGICAL AND GAIT ANALYSIS IN PATIENTS UNDERGOING TOTAL KNEE ARTHROPLASTY USING ULTRACONGRUENT VERSUS CRUCIATE RETAINING BEARING DESIGN

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/05/042474
Enrollment
50
Registered
2022-05-11
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: 7- Osteopathic

Interventions

Intervention1: Ultracongruent bearing: Total knee arthroplasty using Ultracongruent bearing Control Intervention1: Cruciate retaining bearing: Total knee arthroplasty using Cruciate retaining bearing

Sponsors

AIIMS NEW DELHI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults above 50 years and suffering from symptomatic comparable bilateral osteoarthritis knee and undergoing simultaneous bilateral total knee arthroplasty.

Exclusion criteria

Exclusion criteria: 1.Patients with inflammatory arthritis of the knee joint. 2.Patients with post-traumatic arthritis. 3.Patients with spinal, hip or neurological issues affecting gait or stability. 4.Patients with posterior laxity. 5.Patients undergoing simultaneous hip and knee arthroplasty. 6.Patients who refuse to participate in the study. 7.Patients with severe deformities

Design outcomes

Primary

MeasureTime frame
To assess forgotten joint score as a patient reported outcome after TKA surgeryTimepoint: Post-operatively at 2 weeks,1 month,3 months,6 months,1 year—

Secondary

MeasureTime frame
Static and dynamic stability range of motion gait analysis Timepoint: Post-operatively at 2 weeks,1 month,3 months,6 months,1 year—

Countries

India

Contacts

Public ContactKUSHAGRA KUMAR PATHAK

AIIMS,NEW DELHI

rmalhotra62@gmail.com9350020044

Outcome results

None listed

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