Test formula
OtherHydrolyzed rice protein formula
NCT Number: NCT06633250
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).
Interested in participating?
Request InfoUp to 8 month
All sexes
Interventional
Not applicable
Charité Universitätsmedizin Berlin, Berlin, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Hydrolyzed rice protein formula
Commercially available extensively hydrolyzed cow's milk formula
Time frame: 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.
Time frame: Monthly from enrollment to 4 months post-enrollment
Weight (g and z-scores)
Time frame: Monthly from enrollment to 4 months post-enrollment
Length (cm and z-scores)
Time frame: At enrollmentn and 4 months post-enrollment
Head circumference (cm and z-scores)
Time frame: At enrollmentn and 4 months post-enrollment
Tibia (cm)
Time frame: At enrollmentn and 4 months post-enrollment
Femur (cm)
Time frame: Monthly from enrollment to 4 months post-enrollment, and 7 days after enrollment
The Infant Gastrointestinal Symptom Questionnaire (IGSQ) will be used to assess GI tolerance. The IGSQ is a validated instrument that includes 13 questions in 5 domains (stooling, spitting-up/vomiting, crying, fussiness, and flatulence) and total scores range from 13 (best) to 65 (worst) for overall GI symptom burden.
Time frame: First 7 days post enrollment
A daily GI tolerance questionnaire will be used.
Time frame: At enrollment
A retrospective 1-day stool record including the Brussels Infant and Toddler Stool Scale will be used.
Time frame: 2 months and 4 months post-enrollment
A 3-day stool diary including the Brussels Infant and Toddler Stool Scale will be used.
Time frame: Monthly from enrollment to 4 months post-enrollment
The Cow's Milk-related Symptom Score (CoMiSS) will be used to assess symptoms related to CMPA. The CoMiSS questionnaire contains 6 items and generates a score based on gastrointestinal, dermatological, respiratory, and general symptoms (total score range 0-33), which may be associated with CMPA .
Time frame: At enrollment and 4 months post-enrollment
The Food Allergy Quality of Life Questionnaire (FAQLQ-PF) will be used. It is a validated instrument with 30 items in 3 domains (emotional impact, food-related anxiety, dietary and social restrictions).
Time frame: At enrollment and 4 months post-enrollment
Parental self-efficacy in managing their child's food allergy will be assessed using the Food Allergy Self-Efficacy Scale for Parents (FASE-P). The FASE-P is a validated instrument with 21 items.
Time frame: At enrollment and 4 months post-enrollment
Parent-reported infant health-related quality of life will be assessed using the Infant and Toddler Quality of Life Questionnaire - Short Form (ITQOL-SF47). The ITQOL-SF47 is a validated instrument with 47 items.
Time frame: At enrollment, 2 months post-enrollment and 4 months post-enrollment
Total energy and macronutrient intake calculated from food recalls / diaries.
Time frame: Monthly from enrollment to 4 months post-enrollment
A questionnaire will be used to assess formula compliance.
Time frame: 4 months post-enrollment
A questionnaire will be used to assess formula liking.
Time frame: From enrollment to 4 months post-enrollment
Adverse Events will be collected.
Contact information is provided by the study sponsor or research team.
Société des Produits Nestlé (SPN)
Industry
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: a Randomized Nutritional Clinical Study
Acronym: RIGHT-GO
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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