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Clinical Trials/IRCT2014081718832N1
IRCT2014081718832N1Completed未知

Comparing the effects of nasogastric feeding intervals on feeding tolerance in Intensive Care Unit patients

Hamedan university of medical science0 sites63 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
63

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to no limit (—)
Sex
All

Inclusion Criteria

  • Patients are eligible for inclusion if they: are nasogastric tube fed via Bolus infusion; =18 years of age; are expected to have an ICU length of stay (LOS) >3days; don’t have diabetic disease, renal /hepatic failure because they need special formulas such as diabetic formula, hepatic formula; patients who are not immunocompromised; don’t have gastrointestinal diseases or surgery during recent 6 weeks; don’t have drug abuse history; don’t use drugs that increase gastrointestinal motility; don’t have diarrhea before the study. Participants are excluded from the study if they: need gastrointestinal motility enhancing drugs; change of feeding methods or formula during study; have gastric residual volume more than 200 ml; have gastrointestinal complications by another reasons; die or transfer from ICU to another wards; be made NPO due to the diagnostic and therapeutic procedures

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Hamedan university of medical science

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