MedPath

A study in ICU patients to compare ultrasonographic vs manual aspiration techniques for assessment of gastric reserve volume.

Not Applicable
Conditions
Health Condition 1: 4- Measurement and Monitoring
Registration Number
CTRI/2020/10/028261
Lead Sponsor
RAHUL SHARMA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1) Critically ill enterally fed patients.

2) Anticipated ICU stay of atleast 5 days.

3) Not on any prokinetics for feed intolerance.

4) Patients giving consent for participating in the study.

Exclusion Criteria

1) Bowel surgery within 24 hours.

2) Gastrointestinal bleed, obstruction, perforation, malabsorption syndrome.

3) Abnormal Liver function tests; SGOT/ SGPT more than three times normal and/ or total bilirubin more than three times normal.

4) Hemodynamic instability (MAP less than 70).

5) Morbid obesity/ pregnancy (unable to achieve right lateral position).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To find specificity and sensitivity of Ultrasonographic assessment and manual aspiration technique for measurement of GRV. <br/ ><br>Timepoint: All the enterally fed patients fulfilling the inclusion criteria would be subjected to bedside ultrasonography for measurement of gastric reserve volume followed by manual aspiration for the same measurement twice a day at morning and evening prior to feed with last feed atleast 4 hours prior to estimation of GRV. <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
Incidence of gastric feed intolerance in our ICU. <br/ ><br>Assessment of other features of gastric intolerance eg. vomiting, flatulence, diarrhea and stomach ache in the study group. <br/ ><br>Role of Levosulpiride in preventing gastric intolerance. <br/ ><br>Side effects of the drug if used.Timepoint: 12 months
© Copyright 2025. All Rights Reserved by MedPath