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Oral Nutritional Supplementation in Children at Risk of Undernutrition

NCT05161000 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 279

Last updated 2024-07-16

No results posted yet for this study

Summary

The objective of this randomized, controlled trial is to evaluate the effects of consuming a pediatric oral nutritional supplement (ONS) plus dietary counseling for 120 days on anthropometric growth, strength, and nutritional status, compared with dietary counseling alone in undernourished children in the United States.

Conditions

  • Undernutrition

Interventions

OTHER

Oral Nutritional Supplement

ONS plus dietary counseling

OTHER

Dietary counseling

dietary counseling

Sponsors & Collaborators

  • Abbott Nutrition

    lead INDUSTRY

Principal Investigators

  • Jennifer Williams, MPH · Abbott Nutrition

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
36 Months
Max Age
107 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-18
Primary Completion
2024-06-11
Completion
2024-06-11

Countries

  • United States

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 NCT05161000 on ClinicalTrials.gov