Health Condition 1: - Health Condition 2: 4- Measurement and Monitoring
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: a) Age18 years and above b) American Society of Anaesthesiologists (ASA) grade I and II c) Patients scheduled to undergo elective surgery. d) Patients willing to participate and willing to give consent for the study
Exclusion criteria
Exclusion criteria: a) Patient s refusal. b) Patients unable to provide informed consent. c) Patients with risk factors for delayed gastric emptying including Diabetes mellitus, Obesity, Pregnant women, pyloric stenosis, chronic renal failure, History of Gastroeosophageal reflux disease (GERD) or acid peptic disease, Intestinal obstruction or gastrointestinal malignancy. d) Patients with known or suspected allergy/intolerance to the study of clear fluid. e) Patients with neurological disorders (Parkinsons disease, spine cord injury) with altered mental status (Glasgow coma scale <13) f) Patients on medications known to delay gastric emptying (e.g. GLP agonist). g) Non-visualization (e.g. due to gas or obesity)may lead to repeated attempts; persistent failure will result in exclusion.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary To measure and compare the gastric residual volume in patients receiving different types of clear fluids using ultrasound.Timepoint: 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| evaluation of thrist sensation in both the groupsTimepoint: 6 months | — |
Countries
India
Contacts
LILAVATI HOSPITAL MUMBAI