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Pectin Supplemented Enteral Feedings in Critically Ill Patients

NCT04438473 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2021-07-15

No results posted yet for this study

Summary

The current study will enroll critically ill patients who are going to require enteral nutrition support and randomize them to standard formula enteral nutrition or pectin-supplemented enteral nutrition in 7 days. The occurrence of enteral nutrition-related complications will be recorded and compared between groups.

The study is trying to assess whether the use of pectin will improve the enteral nutrition-related complications in critically ill patients.

Conditions

  • Enteral Nutrition
  • Dietary Fiber

Interventions

DIETARY_SUPPLEMENT

pectin-supplemented enteral nutrition feeding

sequential supplementation with combination of 90ml pectin and 500ml enteral nutrition formula for 7 days

OTHER

enteral nutrition feeding

standard formula enteral nutrition feeding without pectin for 7 days

Sponsors & Collaborators

  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    lead OTHER

Principal Investigators

  • Pianhong Zhang, MS · Second Affiliated Hospital, School of Medicine, Zhejiang University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-30
Primary Completion
2020-12-01
Completion
2021-12-01

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04438473 on ClinicalTrials.gov