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Stomach volume in patients undergoing surgery

Not Applicable
Completed
Conditions
Health Condition 1: null- PATIENTS AWAITING ELECTIVE SURGERY
Registration Number
CTRI/2018/01/011558
Lead Sponsor
Dr Jeson R Doctor
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
92
Inclusion Criteria

All adult patients who give consent to participate in the study

Exclusion Criteria

1.Co-morbidities that delay gastric emptying [e.g Diabetics, morbid obesity (BMI >40), Pregnancy, pyloric stenosis]

2.Intestinal obstruction

3.Gastric or Oesophageal malignancy or pathology

4.Therapy with opioids, antacids or prokinetics

5.History of acid peptic disease or gastric reflux

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To measure GRV in 4 groups of patients who have received <br/ ><br>a)No preoperative fluids (at least 8 hours fasting) <br/ ><br>b)200 ml of plain water 2 hoursâ?? prior <br/ ><br>c)200 ml of clear apple juice 2 hoursâ?? prior <br/ ><br>d)200 ml of flavoured ORS 2 hoursâ?? prior <br/ ><br>This will be calculated as the average GRV (mean and SD) for each group as measured by a trained radiologist <br/ ><br>Timepoint: Two hours after ingestion of liquid
Secondary Outcome Measures
NameTimeMethod
1.To determine inter-observer (between observers with different levels of expertise in USG) reliability of ultrasound guided measurement of GRV <br/ ><br>2.To compare the palatability of clear apple juice (Appy) and flavoured ORS (Electral) with plain water, in fasting patients <br/ ><br>Timepoint: Two hours after ingestion of liquid
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