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sonography of the stomach after giving teo types of clear fluid

ULTRASOUND GUIDED ASSESSMENT OF GASTRIC RESIDUAL VOLUME IN PATIENTS RECEIVING TWO TYPES OF CLEAR FLUIDS- OBSERVATIONAL STUDY - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/03/105685
Enrollment
84
Registered
2026-03-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: - Health Condition 2: 4- Measurement and Monitoring

Interventions

Intervention1: Nil: Nil

Sponsors

lilavati hospital
Lead Sponsor

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

MeasureTime frame
Primary To measure and compare the gastric residual volume in patients receiving different types of clear fluids using ultrasound.Timepoint: 6 months

Secondary

MeasureTime frame
evaluation of thrist sensation in both the groupsTimepoint: 6 months

Countries

India

Contacts

Public ContactDR AMI RAJDEV

LILAVATI HOSPITAL MUMBAI

drsatishkulkarni@yahoo.com9821321063

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026