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Recruiting Not applicable

Effect of a Hydrolyzed Rice Protein-based Formula on Growth, Tolerance, and Health-related Quality of Life in Infants With Cow's Milk Protein Allergy.

NCT06633250 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2024-10-25
Last updated
2025-12-26

Condition(s) studied

Cow Milk Protein Allergy

Investigational drug(s) / intervention(s)

Test FormulaControl Formula

Test Formula: Hydrolyzed rice protein formula

Control Formula: Commercially available extensively hydrolyzed cow's milk formula

Study summary

The main purpose of this study is to demonstrate that the growth of infants fed with the Test Formula is non-inferior those fed with the Control Formula. The study will also evaluate the gastrointestinal tolerance, quatliy of life and acceptability of the new rice protein-based formula in infants with cow's milk protein allergy (CMPA).

Eligibility

Sex
ALL
Min age
—
Max age
8 Months
Healthy volunteers
No
Inclusion Criteria: 1. Written informed consent has been obtained from at least one parent (or legally acceptable representative \[LAR\]), if applicable) 2. Infant gestational age ≥ 37 completed weeks 3. Infant birth weight of ≥ 2.5 kg and ≤ 4.5 kg 4. Singleton birth 5. Infant age ≤ 8 months 6. Mother has previously decided to fully formula-feed, and infant is no longer breastfeeding or receiving breast milk 7. Suspected CMPA as per standard clinical practice and in conjunction with at least 2 symptoms present from the list shown below: 1. Inconsolable crying, regurgitation, liquid stools or constipation, skin atopic lesion, cow's milk provoked temporary urticaria/angioedema or vomiting, bloody streaks in stool, or respiratory symptoms 2. For diagnosis based on either a positive IgE blood test, skin prick test or food challenge, only at least 1 symptom from above list needs to be present 8. Infant is receiving a strict cow's milk elimination diet and will continue receiving this diet until the completion of the study 9. Infant's parent(s)/LAR is of legal age of majority, must have parental authority, must understand the informed consent form and other study documents, and is willing and able to fulfill the requirements of the study protocol Exclusion Criteria: 1. History of intolerance to eHF formula 2. Any chronic medical diseases (except atopic eczema), chromosomal or major congenital anomalies (based on medical history and/or commonly performed diagnostic criteria) 3. Major gastrointestinal disease / abnormalities (other than CMPA) 4. Known or suspected lactose intolerance or malabsorption 5. Known or suspected soy allergy 6. Glucose-galactose malabsorption 7. Rice protein allergy or intolerance (e.g., rice protein-induced enterocolitis syndrome). 8. Immunodeficiency 9. Persistent wheeze or chronic respiratory disease 10. Severe uncontrolled eczema 11. History of severe anaphylactic reaction (e.g., requiring ≥ 2 doses of epinephrine) to cow's milk or breast milk at any time prior to enrollment 12. Weight-for-age value \< -2 or \> 2 standard deviations from the WHO Child Growth Standards median at enrollment 13. Height-for-age \< -2 or \> 2 standard deviations from the WHO Child Growth Standards median at enrollment 14. Infant's parent has other medical or psychiatric condition that, in the judgement of the investigator, would make the infant inappropriate for entry into the study 15. Currently participating or having participated in another interventional clinical study within 4 weeks prior to enrollment

Primary outcome measure(s)

  • Weight-for-age z-score at 4 months post-enrollment — From enrollment to 4 months post-enrollment
    Weight measured in g and expressed in z scores according to the World Health Organization (WHO) Child Growth Standards.

Trial sites (19)

FacilityCityRegionStatus
Charité Universitätsmedizin Berlin Berlin Germany Recruiting
Azienda Ospedaliera Universitaria Federico II Naples Italy Recruiting
Azienda Ospedaliero Universitaria di Parma Parma Italy Recruiting
AOUP Ospedale Santa Chiara Pisa Italy Completed
Ospedale Pediatrico Bambino Gesu Rome Italy Not Yet Recruiting
AO Ordine Mauriziano Turin Italy Recruiting
Poliklinika Ginekologiczno-Położnicza Arciszewscy Bialystok Poland Recruiting
Centrum Medyczne Pratia Bydgoszcz Poland Recruiting
IN-VIVO Bydgoszcz Bydgoszcz Poland Recruiting
Prywatna Praktyka Lekarska Gabinet Pediatryczno-Alergologiczny Bydgoszcz Poland Recruiting
Vitamed Galaj i Cichomski Bydgoszcz Poland Recruiting
BioMedical Centers Janki Poland Recruiting
Centrum Medyczne Plejady Krakow Poland Completed
Jagiellonian University Medical College Krakow Poland Recruiting
Wojewodzki Szpital Specjalistyczny im. M. Kopernika Lodz Poland Recruiting
ETG Lublin Lublin Poland Recruiting
Korczowski Bartosz Gabinet Lekarski Rzeszów Poland Recruiting
Alergo-Med Specjalistyczna Przychodnia Lekarska Tarnów Poland Recruiting
University Hospital of Warsaw Warsaw Poland Completed
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06633250 on ClinicalTrials.gov ↗ ← All trials in Italy