To compare the outcome of total knee arthroplasty

Comparison of functional outcome and patient reported outcome in cruciate retaining versus posterior stabilising total knee arthroplasty: A prospective randomised control clinical trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/11/021948

Enrollment

Registered

2019-11-11

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: M170- Bilateral primary osteoarthritis of knee

Interventions

Intervention1: total knee arthroplasty: one group of patients will undergo cruciate retaining total knee arthroplasty and other group will undergo posterior stabilising total knee arthroplasty Control

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patient undergoing b/l total knee arthroplasty during study period using same implant 2)Varus deformity 3)Age between 50 years and 85 years 4)Patient having primary osteoarthritis 5)Patient giving consent for surgery

Exclusion criteria

Exclusion criteria: 1) Revision cases of total knee arthroplasty 2) Post traumatic, post tb knee 3) patients with restricted range of motion 4) patients not giving consent

Design outcomes

Primary

Measure	Time frame
Comparison of functional and patient reported outcome in cruciate retaining versus posterior stabilising total knee arthroplastyTimepoint: 12 months	—

Secondary

Measure	Time frame
1)To assess the FJS and OKS of cruciate retaining tkr 2) To assess the FJS and OKS of posterior stabilising total knee arthroplastyTimepoint: 12 months	—

Countries

India

Contacts

Public ContactROSHAN YADAV

All India Institute Of Medical Sciences,New Delhi

csyadavortho@gmail.com00917982783975

Outcome results

None listed

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