Health Condition 1: M810- Age-related osteoporosis without current pathological fracture Health Condition 2: O- Medical and Surgical Health Condition 3: M171- Unilateral primary osteoarthritisof knee
Conditions
Interventions
Intervention1: Different doses of Dexmedetomidine.: GROUP Aâ?? Ropivacaine with 10mcg of dexmedetomidine
Duration- 0,2,4,6,12 hours
Control Intervention1: Different doses of Dexmedetomidine.: GROUP B-
Sponsors
CHANDINI MISHRA
Eligibility
Inclusion criteria
Inclusion criteria: 1.American society of Anaesthesiologist (ASA) Physical Status I and II posted for elective lower limb surgeries. 2.Patients of age 18-60 years of either sex.
Exclusion criteria
Exclusion criteria: 1.History of allergy to the drugs used in the study like ropivacaine,dexmedetomidine. 2.pregnant women 3.deformity in spine. 4.patients with sinus bradycardia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| â?¢. Postoperative VAS score. Timepoint: 2,4,6,8,12 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.The incidence of hypotension and bradycardia intraoperatively. 2. Time taken for onset of sensory component by using the cold swab test till the loss of sensations.Timepoint: 2HRS,4HRS,6HRS,12HRS. | — |
Countries
India
Contacts
Public ContactCHANDINI MISHRA
KALINGA INSTITUTE OF MEDICAL SCIENCES
Outcome results
None listed