Post operative pain control in super umbilical surgical incision. umbilical surgical incision
Conditions
Interventions
Intervention 1: Intervention group: A high-frequency linear ultrasound probe will be placed in a longitudinal parasagittal orientation at the sixth intercostal space in the anterior midaxillary line.
Sonosite M-Turbo™, Bothell, WA, USA) using a 22G (0.70 mm × 50 mm)Stimuplex® A insulated needle (B. Braun, Melsungen, Germany) via an in-plane approach to the rectussheath. 10 mL of 1% lignocaine, tog
Sponsors
Mansoura university
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: American Society of Anesthesiologists (ASA) physical status grade I -II Scheduled to undergo elective supra-umbilical surgeries under GA (epigastric herniotomy- gastrectomy-open cholecystectomy- nephrectomy).
Exclusion criteria
Exclusion criteria: Allergy to local anesthetics,, Infection at the site of injection, Coagulopathy, Chronic pain syndromes Prolonged opioid medication, Chronic liver disease , or chronic renal disease, cognitive impairment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| POST OPERATIVE PAIN SCORE. Timepoint: 24 hours post operative. Method of measurement: VISUAL ANALUGE SCALE.;Amount of postoperative morphine consumed. Timepoint: 24 hours post operative. Method of measurement: milligram. | — |
Secondary
| Measure | Time frame |
|---|---|
| Amount of postoperative morphine consumed. Timepoint: 24 hours post operative. Method of measurement: milligram. | — |
Countries
Egypt
Contacts
Public ContactZenat Eldadamony
Mansoura university
Outcome results
None listed