Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Erector Spinae Plane Block: 20ml of 0.5% Inj.Bupivacaine with inj.Dexamethasone 8mg
Intervention2: Nil: Nil
Control Intervention1: Control group: No block given
Sponsors
Sapthagiri Institute Of Medical Science and Research
Eligibility
Inclusion criteria
Inclusion criteria: American society of anaesthesiology grade 1&2 Patients posted for unilateral PCNL
Exclusion criteria
Exclusion criteria: Patients not willing to participate in the study. Patients with known allergies to study drug. Contraindications for the subarachnoid block. Patients on any form of chronic pain medications.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to assess the visual analogue score for pain and to determine the time to first rescue analgesiaTimepoint: At baseline,2hrs,4hrs,8hrs,12hrs and 24 hours and to determine the time to first rescue analgesia and compare between both groups. | — |
Secondary
| Measure | Time frame |
|---|---|
| to determine the total analgesic consumptionTimepoint: 24hours | — |
Countries
India
Contacts
Public ContactDR MANJUNATH
Sapthagiri Institute of Medical Science and Research
Outcome results
None listed