ocal Use of Antibiotic Powder during total knee replacement
Not Applicable
Completed
- Conditions
- Health Condition 1: M179- Osteoarthritis of knee, unspecifiedHealth Condition 2: M171- Unilateral primary osteoarthritisof knee
- Registration Number
- CTRI/2021/02/031310
- Lead Sponsor
- Sunshine Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
All adult patients undergoing primary total knee arthroplasty for osteoarthritis of the knee joint
Exclusion Criteria
Inflammatory arthritis
Post-traumatic arthritis
Previous knee surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Acute infection rate: Incidence of Surgical Site Infections (SSI) or Periprosthetic Joint Infection (PJI)Timepoint: Assessment and documentation of surgical site infection (SSI) or Peri-prosthetic Joint Infection (PJI) at 2 weeks, 4 weeks, 3 months, 6 months, 1 year after surgery
- Secondary Outcome Measures
Name Time Method Correlation of patient factors with infection ratesTimepoint: 6 months and 1 year;Functional outcome assessed by Oxford Knee Score (OKS)Timepoint: 3 months, 6 months, 1 year;Functional outcomes assessment by Patient reported outcome measure (PROM) by Forgotten Joint Score (FJS)Timepoint: 3 months, 6 months, 1 year;Functional outcomes using WOMAC scoreTimepoint: 3 months, 6 months, 1 year;Long term Infection rateTimepoint: 1 year;Quality of Life Indicator (EQ-5D)Timepoint: 3 months, 6 months, 1 year