None listed
Conditions
Interventions
Intervention1: Adductor Canal Block: After completion of surgery under spinal anaesthesia, patients in this group will receive an ultrasound-guided adductor canal block. The patient will be kept in su
Sponsors
SRMS IMS
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged 18-70 years of either sex ASA physical status I/II/III
Exclusion criteria
Exclusion criteria: ASA physical status IV Contraindications to spinal anaesthesia Pregnancy Major psychiatric diseases and history of substance abuse Hypersensitivity to study drug- Bupivacaine hydrochloride 0.5% Patient refusal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare visual analogue scale (VAS) scores at different period of time in postoperative period between Adductor canal block group and Femoral nerve block group. To compare range of motion in knee joint as angle of flexion upto 48 hours in the two groupsTimepoint: The patients will be assessed for pain using visual analogue scale (VAS) score and mobility by observing the angle of flexion of knee joint at 1, 2, 3, 6, 12, 24 and 48 hours in the postoperative period. | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare opioid consumption in the two groups in first 48 hours To compare degree of patient satisfaction between the two groupsTimepoint: The patients will also be compared in the two groups based on the opioid consumption in first 48 hours along with the degree of patient satisfaction at the end of the study using an ordinal scale (e.g., very satisfied, somewhat satisfied, dissatisfied, very dissatisfied) | — |
Countries
India
Contacts
Public ContactDr Geeta Karki
Department of Anaesthesia, Shri Ram Murti Smarak Institute of Medical Sciences (SRMS IMS)
Outcome results
None listed