A study to assess sensory loss around knee after total knee replacement surgery
Not Applicable
- Conditions
- Health Condition 1: M179- Osteoarthritis of knee, unspecified
- Registration Number
- CTRI/2024/07/070600
- Lead Sponsor
- Pt. B.D Sharma PGIMS Rohtak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with primary osteoarthritis of the knee who will undergo primary Total knee replacement surgery during the study period will be included
Exclusion Criteria
Previous knee surgery or having a knee scar, Patients having impaired sensation of the knee from any cause, before Total knee replacement e.g. spinal stenosis, recent spine surgery, peripheral neuropathy, peripheral vascular disease etc, Secondary Osteoarthritis of knee, Patients with a valgus deformity around knee, Severe Varus deformity (more than 20 degree) around knee, Inflammatory arthritis of knee, Revision Total knee replacement patients
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method