Health Condition 1: null- American Society of Anesthesiologists Physical status classes 1, 2 Health Condition 2: M171- Unilateral primary osteoarthritisof knee
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ASA 1, 2 patients undergoing unilateral primary total knee replacement arthroplasty
Exclusion criteria
Exclusion criteria: ASA 3,4, bilateral, revision TKR,focal neurological deficits, pre existing peripheral neuropathy,uncontrolled diabetes mellitus,coagulation disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of post operative analgesia as assessed by, 1) VAS (0-10 scale; 0-no pain; 10-worst possible pain) â?¢ pain at rest at 0, 4, 8, 12, 24, 48 hours after surgery â?¢ pain at motion (knee flexion) at 12, 24, 48 hours after surgery 2) Post operative opioid consumption: Total dose of PCA morphine consumed, dose of rescue analgesia used. 3) Duration of analgesia: Time to first use of patient controlled analgesia Timepoint: Quality of post operative analgesia as assessed by, 1) VAS (0-10 scale; 0-no pain; 10-worst possible pain) â?¢ pain at rest at 0, 4, 8, 12, 24, 48 hours after surgery â?¢ pain at motion (knee flexion) at 12, 24, 48 hours after surgery 2) Post operative opioid consumption: Total dose of PCA morphine consumed, dose of rescue analgesia used. 3) Duration of analgesia: Time to first use of patient controlled analgesia | — |
Secondary
| Measure | Time frame |
|---|---|
| Adverse effects of dexmedetomidine in peripheral nerve block such as nausea, vomiting, pruritus, sedation, hypotension, bradycardia, neuropathy in the perioperative period will be recordedTimepoint: Adverse effects of dexmedetomidine in peripheral nerve block such as nausea, vomiting, pruritus, sedation, hypotension, bradycardia, neuropathy in the perioperative period will be recorded | — |
Countries
India
Contacts
All India Institute of Medical Sciences