Health Condition 1: M170- Bilateral primary osteoarthritis of knee Health Condition 2: M174- Other bilateral secondary osteoarthritis of knee Health Condition 3: M175- Other unilateral secondary osteoarthritis of knee Health Condition 4: M171- Unilateral primary osteoarthritisof knee
Conditions
Interventions
Intervention1: Intervention is periarticular injection plus adductor canal block for patients undergoing Total knee Replacement surgery
Comparator is periarticular injection alone in a Total knee Repl
Sponsors
NIL
Eligibility
Inclusion criteria
Inclusion criteria: All patients undergoing Total Knee Replacement surgery
Exclusion criteria
Exclusion criteria: Elderly more than 80 years Revision/Complex Total Knee Replacement Patients with history of Arrhythmia/Cardiac complications Those not willing to give consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain - as estimated by the patients using a numeric pain score till 72 hours post-operativelyTimepoint: 1 At 24 hours after surgery 2 At 48 hours after surgery 3 At 72 hours after surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| 1 Quadriceps strength on post operative day 2,3,5,10 and 3 months- as measured with a standardized load cell,to be recorded by the physiotherapist 2 Time taken to do a Straight Leg Raise with 0 degree lag to a count of 10- without braces - while supine in bed - for each knee 3 Morphine consumption post operatively(Unilateral knees only) 4.Overall satisfaction with pain control peri-operatively ( at time of discharge) (scale of 0-10) Timepoint: 1 At 48 hoursafter surgery 2 At 72 hours after surgery 3 At 5 days after surgery 4 At 10 days after surgery 5 At 3 months after surgery | — |
Countries
India
Contacts
Public ContactDr Nikash P John
Christian Medical College
Outcome results
None listed