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Enhanced Nutrition for Preterm Infants

NCT03238768 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2019-10-29

No results posted yet for this study

Summary

The overall objective of the proposal is to demonstrate the feasibility of providing increased calories and protein in the first week of life to very low birth weight (VLBW) preterm infants.

Conditions

Interventions

OTHER

Enhanced Intravenous Nutrition

Increased macronutrients for first 7 days

OTHER

Standard Intravenous Nutrition

Standard macronutrients for first 7 days

Sponsors & Collaborators

Principal Investigators

  • Sara E Ramel, MD · University of Minnesota Masonic Children's Hospital

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Model
PARALLEL

Eligibility

Max Age
30 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-15
Primary Completion
2019-07-31
Completion
2019-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

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 NCT03238768 on ClinicalTrials.gov