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A comparison of bolus and continuous feeding with respect to vasopressor requirements in sepsis and septic shock patients.

Not Applicable
Conditions
Health Condition 1: A419- Sepsis, unspecified organism
Registration Number
CTRI/2021/07/034796
Lead Sponsor
FORTIS ESCORTS HEART INSTITUTE
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Adults > 18 years of age

2.Patients of sepsis and septic shock as per sepsis 3 definition

3.Admitted to ICU with Nasogastric, Orogastric or Nasojejunal tube for enteral feeding.

4.Patient informed and consented to be included in the study.

5.Patient will be enrolled in the study within 6 hours of start of enteral feeding.

Exclusion Criteria

1.Patient on parenteral nutrition

2.Active bowel obstruction as diagnosed clinically

3.Mesenteric ischemia

4.GI infection precluding Enteral Nutrition

5.Any other contraindications to Enteral nutrition

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.change in vasopressor dose over 1st 72 hours of EN <br/ ><br>2.Addition of any vasopressor drug in order to maintain MAP â?¥65mm of Hg. <br/ ><br>3.Serum lactate level as a marker of hypoperfusion <br/ ><br>Timepoint: every 12th hour until 72 hours
Secondary Outcome Measures
NameTimeMethod
Incidence of gastro intestinal tract complications <br/ ><br>1. Dairrhoea defined as having â?¥ 3 stools (loose/ liquid), with a stool weight 200 grams per day <br/ ><br>2.Vomiting <br/ ><br>3.Gastric residual volume , defined as aspirate volume 500 ml from feeding tube. <br/ ><br>4.Incidences of NOMI & NOBN <br/ ><br>5.ICU length of stay <br/ ><br>6.Discharged from hospital or Death. <br/ ><br>Timepoint: till 72 hours and then during discharge from ICU or hospital
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