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Assessment of Gastrointestinal Discomfort and Infections in Healthy Term Infants (MESK-1)

A

Ausnutria Hyproca

Status

Active, not recruiting

Conditions

Infection
Gastrointestinal Symptoms
Growth
Allergy Symptoms

Treatments

Other: Infants fed goat milk-based infant formula

Study type

Observational

Funder types

Industry

Identifiers

NCT06744699
P24-151

Details and patient eligibility

About

A retrospective observational medical dossier-based study to assess gastrointestinal discomfort and infections in healthy term infants

Full description

Gastrointestinal (GI) symptoms like regurgitation, unexplained crying and stool issues (diarrhoea or constipation) are common in young infants <4 months of age due to an immature gut epithelial barrier, immune system and microbiota, with studies indicating prevalences ranging from 25.9%-78%. This retrospective observational medical dossier-based study is designed to determine the occurrence of GI symptoms in healthy term formula-fed infants to confirm reported prevalence of mild GI symptoms by HCPs in Middle East (74%). As a secondary objective, the improvement of confirmed GI symptoms when switched before 4 months of age from a CMF to GMF will be determined. Based on the results of a previous study in infants with confirmed GI symptoms, it is expected that fewer GI symptoms will be scored in medical dossiers of infants after switching from CMF to GMF, with HM as a reference group. Other secondary objectives of this study are to explore differences between healthy term infants that were fed GMF compared to infants fed CMF or HM on immune related outcomes such as infections and allergies, medication use related to infections and/or gastrointestinal discomfort and/or allergies, number of clinic visits, adequate growth and reason of changing infant formula.

Enrollment

300 estimated patients

Sex

All

Ages

Under 24 months old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Either exclusively formula fed (GMF or CMF; consumption of HM ≤2 weeks is allowed for formula fed infants) OR exclusively breastfed before introduction of complementary feeding.
  • Age 12-24 months of age to ensure collection of recent data.
  • If required by local regulation or guidelines, written informed consent (ICF) from Investigator (or parent(s) and/or caregiver(s)* aged ≥18 years).
  • Singleton, term infants (gestational age ≥ 37 weeks and ≤ 42 weeks).
  • At least 6 reported visits to the doctor between 0-12 months of age.

Exclusion criteria

  • Consumed hydrolysed infant formula or other specialty formulas.
  • Any current or previous illnesses/conditions and/or known congenital diseases or malformations which could interfere with the study outcomes, as per Investigator's clinical judgement.
  • Participation in any clinical trial during first year of life.
  • For formula-fed infant, no switch in feeding type after 4 months of age is allowed.

Trial design

300 participants in 1 patient group

Formula-fed infants
Description:
Formula-fed infants either goat milk-based infant formula or cow's milk-based infant formula
Treatment:
Other: Infants fed goat milk-based infant formula

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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