SMASH: Study to Evaluate the Clinical Efficacy of an Extensively Hydrolysed Infant Formula With Synbiotics and a Human Milk Oligosaccharide (HMO) in Infants With Cow's Milk Protein Allergy (CMPA)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Cow's Milk Protein Allergy (CMPA), Food Hypersensitivity, Infant Nutrition Disorders, Gut Microbiota. Basic parameters: up to 10 months · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Spain
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Cow's milk protein allergy (CMPA) is one of the most common food allergies in infants, with an estimated prevalence between 2% and 5%. The number of diagnosed cases has increased in recent years, with clinical manifestations involving the gastrointestinal tract, respiratory system, skin, or systemic reactions. Dietary elimination of cow's milk protein remains the mainstay of treatment, using extensively hydrolyzed formulas (EHF) or amino acid-based formulas (AAF), depending on the severity of the allergy. This study aims to evaluate the clinical effect, as reported by physicians, of an extensively hydrolyzed whey-based formula (Almirón Pepti Syneo®) containing a symbiotic mixture (scGOS/lcFOS 9:1 and Bifidobacterium breve M-16V), the human milk oligosaccharide 2'-fucosyllactose (2'-FL), and a reduced amount of purified lactose, in infants with suspected or confirmed CMPA in a real-world clinical practice setting. This is a prospective, longitudinal, open-label, single-arm, multicenter study including approximately 41 infants under 10 months of age at several primary care centers and one hospital in Valencia, Spain. Each participant will be followed for four weeks. A subgroup of participants will also provide stool samples to explore the effect of the study formula on gut microbiota composition.
Detailed description
Background and Rationale
Cow's milk protein allergy (CMPA) is a frequent condition in pediatric populations and a major cause of medical consultation during early infancy. Although prevalence estimates vary across studies, it is generally reported between 2% and 5%. CMPA can present with cutaneous, gastrointestinal, respiratory, or systemic symptoms and may impact growth, nutritional status, and family quality of life.
The cornerstone of management is dietary elimination of cow's milk protein. In infants requiring formula feeding, extensively hydrolyzed formulas (EHF) or amino acid-based formulas (AAF) are recommended, depending on allergy severity. Recent evidence suggests that gut microbiota composition plays a key role in the development and modulation of allergic diseases, and that prebiotics, probiotics, and synbiotics may beneficially modulate immune responses via the gut microbiome.
Almirón Pepti Syneo® is an extensively hydrolyzed whey-based formula that includes a symbiotic mixture (scGOS/lcFOS 9:1 and Bifidobacterium breve M-16V), the human milk oligosaccharide 2'-fucosyllactose (2'-FL), and a reduced content of purified lactose. Previous studies have demonstrated its safety, efficacy in managing CMPA symptoms, and support for adequate infant growth.
Objectives
Primary Objective:
\- To evaluate the effect of an extensively hydrolyzed formula containing synbiotics and 2'-FL on physician-reported outcomes related to CMPA symptoms (cutaneous, respiratory, gastrointestinal, and/or systemic) in infants with suspected or confirmed CMPA.
Secondary Objectives:
* To assess parent- or caregiver-reported outcomes related to CMPA symptoms. * To evaluate the impact of the infant's condition on parental or caregiver quality of life. * To describe infant growth during the study period. * To assess parental acceptability and satisfaction with the study product.
Exploratory Objective:
\- To explore the effect of the study formula on gut microbiota composition and stool characteristics in infants with suspected or confirmed CMPA.
Study Design
This is a prospective, longitudinal, open-label, single-arm, multicenter study conducted at approximately 13 primary care centers and one hospital (Hospital Quirón, Valencia, Spain). The study will enroll 41 infants under 10 months of age with suspected or recently confirmed CMPA.
Each infant will be followed for four weeks after the initiation of the study formula. Parents or legal guardians will complete standardized and ad hoc questionnaires regarding symptom evolution, gastrointestinal function, and product acceptability, while investigators will record clinical and anthropometric data using an electronic case report form (eCRF).
A subgroup of infants whose parents or guardians consent to the exploratory stool analysis will provide samples for microbiota assessment, processed at the sponsor's laboratories in Singapore and Utrecht.
Sample Size and Study Population
A total of 41 infants under 10 months of age with suspected or recently diagnosed CMPA will be recruited, assuming a 30% potential dropout rate. Infants with prior use of EHF, AAF, rice hydrolysate, or soy formulas will be excluded.
Variables
Collected data will include:
* Sociodemographic and baseline characteristics: sex, birth weight and length, gestational age, family history of allergy, feeding type, and antibiotic use. * Anthropometric measures: weight, length, and head circumference at baseline and study end. * Clinical assessments: CoMiSS, SCORAD, and IGSQ-13 scores. * Parent-reported outcomes: ad hoc symptom and stool questionnaires, PO-SCORAD, FAQL-PB, and acceptability/satisfaction surveys. * Safety: adverse events and concomitant medications.
Study Duration
Recruitment will take place over approximately nine months. Each participant will be followed for four weeks.
Primary outcome measures
- Change in investigator-reported allergy symptom scores [Time frame: Baseline (Visit 1) and Week 4 (Visit 2)]
Secondary outcome measures (5)
- Change in parent-reported allergy symptom scores from baseline to Week 4 [Time frame: Baseline and Week 4]
- Change in stool characteristics from baseline to Week 4 [Time frame: Baseline and Week 4]
- Change in parental quality of life related to infant allergy from baseline to Week 4 [Time frame: Baseline and Week 4]
- Change in infant anthropometric z-scores from baseline to Week 4 [Time frame: Baseline and Week 4]
- Parental acceptability and satisfaction with the study formula [Time frame: At Week 4]
Eligibility criteria
Inclusion criteria
- Infants under 10 months of age at study start (Visit 1).
- Suspected or recently confirmed cow's milk protein allergy (CMPA), as determined by the investigator.
- Already formula-fed, or parents/legal guardians have decided to initiate formula feeding.
- Inclusion in the study coincides with the first prescription of a hypoallergenic formula.
- Written informed consent obtained from parents or legal guardians in accordance with local regulations.
Exclusion criteria
- Infants with functional gastrointestinal symptoms in whom atopy or food allergy is not suspected.
- Infants who have previously used an extensively hydrolyzed formula (EHF), an amino acid-based formula (AAF), a rice hydrolysate formula, or a soy-based formula.
- Infants who have previously used a partially hydrolyzed formula for the prevention of cow's milk protein allergy (CMPA).
- Infants for whom an amino acid-based formula (AAF) is more appropriate as first-line management, including severe forms of CMPA.
- Contraindications to the use of synbiotics (e.g., preterm infants <40 weeks of corrected gestational age at study start, immunodeficiency, short bowel syndrome, parenteral nutrition, post-pyloric feeding, central venous catheter, oncology treatment, or graft-versus-host disease).
- Any other condition, as assessed by the investigator, that contraindicates the use of an extensively hydrolyzed formula.
- Any other circumstance, as assessed by the investigator, indicating that the parents or legal guardians are not capable of complying with the study procedures.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Spain · 13 centers
- Quironsalud Valencia Hospital — Valencia
- Trinitat Health centre — Valencia
- Malva-rosa Health centre — Valencia
- República Argentina Health centre — Valencia
- Salvador Pau Health centre — Valencia
- Serrería 2 Health Centre — Valencia
- Serrería I Health Centre — Valencia
- Trafalgar Health centre — Valencia
- … and 5 more centers
Identifiers
NCT: NCT07342621 · NUT-2023-185-APLV