Skip to content

Thirty day post operative complications following primary total knee replacement

A prospective observational study on thirty day post operative complications following primary total knee replacement surgery - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100062
Enrollment
30
Registered
2026-01-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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: Total knee arthroplasty is a surgical procedure of approximately 90 minutes performed in patients With osteoarthritis of knee joint Control Intervention1: Nil:

Sponsors

Dr. Sumit Tibrewal
Lead Sponsor
Department of Orthopaedics PGIMS Rohtak
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing primay Total knee arthroplasty

Exclusion criteria

Exclusion criteria: Patient undergoing total knee arthroplasty for hemophilia arthropathy and malignant disease. Patient undergoing revision surgery. Patient undergoing hybrid total knee arthroplasty with all polyethylene tibial components will be excluded from the study

Design outcomes

Primary

MeasureTime frame
2011 Knee Society score, Western Ontario and McMaster Universities Osteoarthritis Index WOMACTimepoint: Scores measured pre operative and post operative at first month

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDr Pradeep kamboj

PGIMS Post Graduate Institute of Medical Sciences Rohtak

kambojdr@gmail.com9992014147

Outcome results

None listed

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