Health Condition 1: M171- Unilateral primary osteoarthritisof knee Health Condition 2: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Unilateral Total Knee Replacement patients Patients willing to provide informed consent
Exclusion criteria
Exclusion criteria: Allergy to study medications Extensive soft tissue release Severe varus deformity (HKA greater than10 ) Inflammatory arthritis Painful hip pathology Intraoperative fracture Previous steroid injection into knee Revision surgery Previous surgery around knee
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative pain assessed using the Visual Analog Scale (VAS)Timepoint: 2 hours , 4 hours , 8 hours , 12 hours , 24 hours and 48 hours after the completion of surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| VAS Score at 2, 4, 8, 12 and 48 hours postoperatively.Timepoint: 2, 4, 8, 12, and 48 hours;Requirement of rescue analgesia (Intravenous Tramadol 100mg)Timepoint: ;Frequency of rescue analgesia during first 48 hours postoperativelyTimepoint: First 48 postoperative hours;Range of motion at 4, 12 24, 48 and 72 hours postoperativelyTimepoint: 4, 12, 24, 48, and 72 hours postoperatively;Time to breakthrough pain ( VAS greater than or equal to 5)Timepoint: ;Cumulative opioid consumptionduring first 48 postoperative hours.Timepoint: | — |
Countries
India
Contacts
All India Institute of Medical Sciences , Patna