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Does a Clinical Support System for Parenteral Nutrition (PN) Facilitate the Judgement on Choosing the Most Effective Commercial Solution Per Patient (and Modify it, if Necessary)? (CDSS)

I

Iaso Maternity Hospital, Athens, Greece

Status

Completed

Conditions

Clinical Decision Support System

Treatments

Other: CDSS Canceling

Study type

Interventional

Funder types

Other

Identifiers

NCT05670613
19042020

Details and patient eligibility

About

Standard formulas of PN have been developed and provided to patients. Only few randomized controlled studies compared standardized vs individualized PN. Individually tailored PN, only if standard PN solutions do not meet patient's nutritional needs. ASPEN society recommends the use computerized prescribing. Technology has enabled the incorporation of medical guidelines in CDSSs. New approach: Comparison of patient's calculated nutritional needs with commercial available solutions.

Enrollment

67 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitalize Patients unable to be fed via gastrointestinal tract.
  • Hemodynamically stable patients.
  • PN regimen should remain the same for the first 3 days.

Exclusion criteria

  • Hemodynamically unstable.
  • Anticipated need for parenteral nutrition less than 5 days.

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

67 participants in 2 patient groups

Dispense Ready to Use PN Solutions
Other group
Description:
Dispensed to patient commercial solution.
Treatment:
Other: CDSS Canceling
Dispense the most effective commercial Solution calculated with the use of the CDSS
Other group
Description:
Dispensed to patient the most effective commercial solution after the CDSS calculations.
Treatment:
Other: CDSS Canceling

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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