Difference between drugs in critically ill patient with enteral feed intolerance.
Not Applicable
- Conditions
- Health Condition 1: R00-R99- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified
- Registration Number
- CTRI/2024/02/062858
- Lead Sponsor
- Eras Lucknow medical college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Critically ill patients admitted in ICU who had enteral feed intolerence.
Patients of either sex
Patients of age group 18-75 year
Exclusion Criteria
Patients with allergy to study drugs.
Treatment with any prokinetics drugs 24 h before participating in the study.
Hemodynamic instability or presence of cardarrhythmia or prolonged QT interval .
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PRIMARY OBJECTIVES: <br/ ><br>The rate of successful feeding at 48 hours after randomization. <br/ ><br>Timepoint: 48 hours.
- Secondary Outcome Measures
Name Time Method Icu length of stay <br/ ><br>Hospital length of stay <br/ ><br>Timepoint: Icu length of stay <br/ ><br>Hospital length of stay