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Pectin Supplemented Enteral Feedings in Critically Ill Patients

The Effect of Pectin Supplement on Enteral Nutrition-related Complications in Critically Ill Patients

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04438473
Enrollment
0
Registered
2020-06-18
Start date
2020-07-30
Completion date
2021-12-01
Last updated
2021-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dietary Fiber, Enteral Nutrition

Brief 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.

Interventions

DIETARY_SUPPLEMENTpectin-supplemented enteral nutrition feeding

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

OTHERenteral nutrition feeding

standard formula enteral nutrition feeding without pectin for 7 days

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged 18-80 years old, with informed consent to participate; * Critically ill patients who require enteral nutrition support

Exclusion criteria

* Patients with lung infection at admission * Condition which contraindicates enteral feeding (i.e. intestinal obstruction) * Lack of enteral access * Any condition that would contraindicate use of the enteral nutrition * Require enteral nutrition support for less than 1week or more than 4 weeks from enrollment

Design outcomes

Primary

MeasureTime frameDescription
Complication of enteral feeding7 daysRecord daily diarrhea ,complications, aspiration pneumonia,poor gastric emptying

Secondary

MeasureTime frameDescription
feeding time of enteral nutrition7 daysRecord daily feeding time of enteral nutrition
total energy intake7 daysRecord daily energy intake

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026