NCT01658267 is a Phase 3 clinical trial of nutritional supplement in Children, sponsored by Abbott Nutrition.

Who is sponsoring NCT01658267?

NCT01658267 is sponsored by Abbott Nutrition.

What drugs are being tested in NCT01658267?

Interventions in NCT01658267: nutritional supplement.

What condition does NCT01658267 study?

NCT01658267 studies Children, Under-nutrition.

Is NCT01658267 still recruiting?

NCT01658267 is currently completed. Last updated 19 January 2015.

Last reviewed 2015-01-19 · How we verify

NCT01658267

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

Compliance With Dietary Recommendations in Meeting Nutritional Requirements in Children at Risk of Undernutrition

Completed Phase 3 Last updated 19 January 2015

What this trial tests

Phase 3 trial testing nutritional supplement in Children in 200 participants. Completed in 1 October 2012.

Timeline

1 October 2011

Primary endpoint
1 October 2012

1 October 2012

Quick facts

Lead sponsor	Abbott Nutrition
Phase	Phase 3
Status	Completed
Study type	INTERVENTIONAL
Allocation	na
Design	single group
Masking	none
Primary purpose	treatment
Enrollment	200
Start date	1 October 2011
Primary completion	1 October 2012
Estimated completion	1 October 2012
Sites	2 locations across Philippines

Drugs / interventions tested

nutritional supplement — full drug profile →

Conditions studied

Children — all drugs for Children →
Under-nutrition — all drugs for Under-nutrition →

Sponsor

Abbott Nutrition — full company profile →

Who can join

Adults 36 Months to 48 Months, any sex, with Children or Under-nutrition. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Compliance with recommendation of a nutritional supplement consumption
Time frame: 48 weeks

Sponsor's own description

This study will assess compliance with dietary recommendations, in conjunction with a nutritional supplement to meet the nutritional requirements in children and the effects of the compliance on promoting growth in children who are at risk of under-nutrition.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

Longitudinal growth and health outcomes in nutritionally at-risk children who received long-term nutritional intervention.
Huynh DT, Estorninos E, Capeding RZ, Oliver JS, et al · · 2015 · cited 25× · PMID 25808062 · DOI 10.1111/jhn.12306
Impact of long-term use of oral nutritional supplement on nutritional adequacy, dietary diversity, food intake and growth of Filipino preschool children.
Huynh DT, Estorninos E, Capeding MR, Oliver JS, et al · · 2016 · cited 8× · PMID 27293557 · DOI 10.1017/jns.2016.6

Verify or expand the search:

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Other Abbott Nutrition trials

Trials by the same sponsor.

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Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT01658267 (US National Library of Medicine, public domain)
Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Abbott Nutrition
Last refreshed: 19 January 2015

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01658267.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing