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This study will investigate the effect of two oral nutritional supplements (ONS) along with dietary counseling vs dietary counseling alone on growth among picky eating children from India, aged > 24 months to ≤ 48 months over a period of 90 days.
Full description
Study Objective:
To investigate the effect of two oral nutritional supplements (ONS) along with dietary counseling vs dietary counseling alone on growth among picky eating children from India, aged > 24 months to ≤ 48 months over a period of 90 days.
Number of Subjects / Length of Participation:
Approximately 321 subjects (107 subjects per group) will be enrolled from estimated 8-10 study centers to obtain at least 255 evaluable subjects (85 subjects per group), assuming 20% attrition rate. Expected total duration for the study is approximately 12 months.
Study Design :
Enrollment
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Inclusion criteria
Child is > 24 months and ≤ 48 months of age at visit 1.
Child of either gender (Male and Female).
Child has a weight-for-height between 3rd - 15th percentiles according to current WHO Growth Charts at visit 1. (WHO Growth Chart 2007)
Child is a picky eater, defined as meeting at least two of the following criteria. A child, who:
Child is a habitual milk drinker at least 1 glass (approximately 200mL) of milk daily.
Child is able to consume foods and beverages orally.
Child's Legal Guardian (LG) or parent(s) is willing to abstain from giving additional non-study nutritional supplements including vitamin/mineral supplements, micronutrient fortified beverages, oral nutritional supplements other than the study product during the study intervention period.
Child's Legal Guardian (LG) or parent(s) has voluntarily signed and dated an informed consent form (ICF), approved by an Independent Ethics Committee/Institutional Review Board (IEC/IRB) prior to any participation in the study.
Child's Legal Guardian (LG) or parent(s) is able and willing to follow study procedures and record data in parent diary and complete any forms or assessments needed throughout the study.
Child's Legal Guardian (LG) or parent(s)is not planning to relocate during the study period
Exclusion criteria
Primary purpose
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Interventional model
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321 participants in 3 patient groups
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Data sourced from clinicaltrials.gov
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