Health Condition 1: M179- Osteoarthritis of knee, unspecified
Conditions
Interventions
Intervention1: Primary total knee replacement surgery: Standard primary total knee replacement done through medial parapatellar approach
Intervention2: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
Pt. B.D Sharma PGIMS Rohtak
Eligibility
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Calculate the incidence of cutaneous hypoesthesia around knee after primary knee replacement surgeryTimepoint: At two weeks, one month, two months and three months minimum | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate early functional outcomes after primary total knee arthroplastyTimepoint: minimum three months after surgery or later;correlation of PROMs (Patient reported outcome measures) {Forgotten Joint Score}[ FJS 12] with cutaneous hypoesthesiaTimepoint: minimum three months after surgery or later;Evaluate association of various risk factors with cutaneous hypoesthesiaTimepoint: At two weeks, one month, two months & three months minimum | — |
Countries
India
Contacts
Public ContactSourabh
Pt B D S PGIMS, Rohtak
Outcome results
None listed