Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: External oblique intercostal Planeblock: Study duration: 2 years (may 2024- may 2026)
Under ultrasound guidance, Regional anesthesia - External oblique intercostal Plane Block will be p
Sponsors
ParkaviV
Eligibility
Inclusion criteria
Inclusion criteria: Age above 18 and below 70 Physical status classification:ASA1and ASA2 Both male and female Patients who are willing to participate
Exclusion criteria
Exclusion criteria: Patients refusal Allergic to local anaesthetic History of multiple previous abdominal surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the analgesic effect of Externaloblique intercostal Planeblock with 0.5% Ropivacaine in laproscopic right donor nephrectomy.Timepoint: Pain is evaluated using Numerical rating scale at the time of extubation and at 1 hr, 3 hrs, 6 hrs, 12 hrs after extubation | — |
Secondary
| Measure | Time frame |
|---|---|
| To determine the efficacy of external oblique intercostal Planeblock & local infiltration in reducing the usage of opioidsTimepoint: Opioids usage time is noted at 3,6,12 hrs after extubation | — |
Countries
India
Contacts
Public ContactParkaviV
Kovai Medical Center and Hospital
Outcome results
None listed