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Effects of Oral Nutritional Supplementation in Children at Risk of Undernutrition

NCT05239208 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 330

Last updated 2023-02-28

No results posted yet for this study

Summary

This prospective, randomized, controlled study will evaluate the effects of oral nutritional supplementation plus dietary counseling versus dietary counseling alone in children at nutritional risk.

Conditions

  • Undernutrition

Interventions

OTHER

Oral Nutrition Supplement (ONS) Group

Oral nutritional supplement specifically designed for nutritionally-at risk children and dietary counseling

OTHER

Control Group

Dietary counseling

Sponsors & Collaborators

  • Abbott Nutrition

    lead INDUSTRY

Principal Investigators

  • Yen Ling Mandy Ow, PhD · Abbott

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
24 Months
Max Age
60 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-14
Primary Completion
2022-12-18
Completion
2022-12-18

Countries

  • Vietnam

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 NCT05239208 on ClinicalTrials.gov