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NCT Number: NCT07549360

Leveraging Optimal Tolerance in Undernourished Infants to Support Growth

The goal of this study is to learn if InfaCore (IC) an energy and nutrient dense formulation (ENDF) can improve growth and tolerance in infants with or at risk of growth faltering when fed IC.

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Key information

Age range

1 month–12 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Pediatrics, Faculty of Medicine, Chulalongkorn University

Bangkok, 10330, Thailand

Location contact

Chonnikant Visuthranukul, MD, PhD

CONTACT

[email protected]

+66 2256 4000 ext. 4903

About this study

Rationale: The definition of FG/FTT was established by a group of experts in a report published in 2023 (Cooke et al., 2023). In this report they agreed a fall in weight-for-age z-score (WAZ) of ≥1.0 SD over a period of 1 or more months (excluding the first 2 weeks after birth) which includes at least 2-3 growth measurements (Cooke et al., 2023). It is also important to consider infants at risk who have static weight for extended periods e.g., >/=4 weeks. FG/FTT affects different populations and is estimated to be 10% of infants globally.

InfaCore (IC) an energy and nutrient dense formulation is indicated for infants and young children with FG/FTT defined above or for those at risk of developing e.g., with static weight for extended periods. At risk infants might include some or all of the following those with congenital heart disease (CHD) admitted for surgical procedures, those with critical illness (CI) or on the PICU, infants cystic fibrosis (CF) or other respiratory conditions including chronic lung disease (CLD), some forms of severe cerebral palsy (CP), and those requiring a surgical procedure or post-surgery.

Objective: To demonstrate growth and tolerance in infants with or at risk of growth faltering when fed IC an Energy and Nutrient Dense Formula (ENDF).

Study design: A prospective, single-centre, single-arm open label pilot study to show growth and tolerance in infants with/at risk of FG/FTT when fed an ENDF for 8 weeks.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Infants aged from 1 month to </=12 months of age
  • Infants taking at least 50% of daily intake from infant formula
  • Diagnosis of FG (a fall in WAZ of ≥1.0 SD over 1 month or more - not including the first 2 weeks after birth) or risk of FG (static weight for >/= 1 month)
  • Infants >/=37 weeks gestation at time of recruitment
  • Parent/ legal guardian willing to provide written informed consent

Exclusion criteria

  • Exclusively Breastfed infants
  • Infants with other medical problems that might independently affect intake (oral or otherwise) or who have specific nutrient needs not met by IC e.g. some gastrointestinal malformations, some renal and liver conditions, inborn errors of metabolism, galactosemia
  • Infants on total parenteral nutrition
  • Infants with cow milk protein allergy
  • Infants with soy allergy
  • Infants who participated in other studies within 2 weeks prior to recruitment
  • Situations where the investigator has concerns about the willingness or ability of the parents/caregivers to comply with protocol requirements
  • Infants who are on a vegan diet
  • Infants who are allergic to fish
  • Infants born preterm <37 weeks gestation

Treatment and study plan

Infant Formula

Other

Prospective, single-center, single-arm open label pilot study to show growth and tolerance in infants with/at risk of FG/FTT when fed an ENDF for 8 weeks.

Other names: Energy and Nutrient Dense Infant Formula (ENDF)

Primary outcomes

  1. Body Weight

    Time frame: 8 weeks

    Body Weight

  2. Change in body weight

    Time frame: 8 weeks

    The primary outcome is the change in weight-for-age Z-score from baseline to study completion, regardless of whether the value increases or decreases.

Study contacts

Contact information is provided by the study sponsor or research team.

Chonnikant Visuthranukul, MD, PhD

CONTACT

[email protected]

+66 2256 4000 ext. 4903

Eakkarin Mekangkul, MD

CONTACT

Sponsors and collaborators

Lead sponsor

Dutch Medical Food

Industry

Registry information

Acronym: LOTUS

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Apr 24, 2026
Registry last updated
Apr 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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