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Effect of an Innovative BIO Formula Intake on Infant Growth and Tolerance From 0 to 6 Months (TRUEGREEN)

20 de abril de 2022 atualizado por: Jean-Michel Lecerf, Institut Pasteur de Lille

Evaluation of an Innovative BIO Formula Based on a New Whey Extraction Process on the Growth and Tolerance of Infants From 0 to 6 Months.

From birth to 5 months, milk is the essential and unique food of the newborn. The French National Nutrition Program (PNNS) recommends exclusive breastfeeding "up to 6 months and at least 4 months for a healthy benefit". However, only 36% of infants 0-6 months of age are exclusively breastfed worldwide. Some mothers choose to give infant formula to their baby in the first few months of life. This decision may be a personal choice or be imposed by pathophysiological situations.

The nutritional requirements of the infant are specific, which implies adequate nutrition. Infant formulas and follow-up formulas are therefore complex products, specially developed for a group of vulnerable consumers. In fact, the compositional and information requirements for infant formula are highly regulated.

This study, defined as a pilot study, proposes to evaluate the innovative "TrueGreen" BIO infant formula based on a new whey extraction method on the growth and tolerance of infants from 0 to 6 months compared to the conventional BIO infant formula. As no growth and tolerance data are currently available for this new TrueGreen BIO formula, this study aims to determine them.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Real)

100

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Nord
      • Lille, Nord, França, 59019
        • NutrInvest - Institut Pasteur de Lille

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

1 dia a 3 semanas (Filho)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • 0 to 3 weeks
  • Child followed by a general practitioner or pediatrician
  • Informed consent form signed by the legal representatives of the subject
  • Commitment of legal representatives to follow the constraints generated by the study
  • Insured

Exclusion Criteria:

  • Infant born prematurely before 37 weeks of amenorrhea
  • Child allergic to cow's milk proteins
  • Pathological pregnancy (hypertension, infection, gestational diabetes, etc.);
  • Chronic or acute illness (metabolic or neuromuscular diseases, epilepsy, asthma, diabetes, digestive, renal, cardiac or haematological diseases);
  • Incapacity for the legal representative(s) to understand or adhere to the protocol
  • Subject involved in another clinical study or in an exclusion period from another study
  • Legal representatives deprived of liberty
  • Legal representatives in a position to judicial protection
  • Weight of the subject according to age and sex, not included between the 3rd and the 97th percentile of the WHO Child Growth Standards
  • Subject height according to age and sex, not between the 3rd and the 97th percentile of the WHO Child Growth Standards
  • BMI of the subject according to age and sex, not included between the 3rd and the 97th percentile of the WHO Child Growth Standards
  • Head circumference of the subject according to age and sex, not included between the 3rd and the 97th percentile of the WHO (World Health Organization) Child Growth Standards
  • The investigator considers that the state of health or the concomitant treatments are not compatible with the good progress of the clinical study.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Outro
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Dobro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador de Placebo: Breast milk
group receiving breastfeeding
Infants were breastfed during 3 months minimum. Data on growth and tolerance were collected. 10 out of 40 infants take a blood test to metabolome analysis
Comparador Ativo: infant formula conventional BIO
infant formula with conventional whey BIO
Infant were fed during 6 months with a conventional BIO infant formula. Data on growth and tolerance were collected. 10 out of 40 infants take a blood test to metabolome analysis
Comparador Ativo: infant formula BIO TrueGreen
infant formula with whey BIO TrueGreen
Infant were fed during 6 months with the TrueGreen BIO infant formula. Data on growth and tolerance were collected. 10 out of 40 infants take a blood test to metabolome analysis

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Evolution of growth of infants
Prazo: from 0 to 6 months
Weight in kilograms
from 0 to 6 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Height evolution of infants
Prazo: from 0 to 6 months
data in centimeters
from 0 to 6 months
BMI evolution of infants
Prazo: from 0 to 6 months
data in kg/m²
from 0 to 6 months
Head circumference evolution of infants
Prazo: from 0 to 6 months
data in centimeters
from 0 to 6 months
Number of colic per day
Prazo: from 0 to 6 months
Evaluation during 3 consecutives days every month.
from 0 to 6 months
Consistency of stool
Prazo: from 0 to 6 months

Evaluation during 3 consecutive days every month via Bristol scale.

According to the bristol scale, seven types of stool are considered:

Type 1: Separate hard lumps, like nuts (hard to pass) Type 2: Sausage-shaped, but lumpy Type 3: Like a sausage but with cracks on its surface Type 4: Like a sausage or snake, smooth and soft Type 5: Soft blobs with clear cut edges (easy to pass) Type 6: Fluffy pieces with ragged edges, a mushy stool Type 7: Watery, no solid pieces, entirely liquid

The mean of stool type during 3 days is considered.

from 0 to 6 months
Number of regurgitation
Prazo: from 0 to 6 months

Evaluation during 3 consecutive days every month via Vandenplas scale.

According to the Vandenplas scale, seven score are considered:

0 0-2 episodes/day

  1. ≥3-≤5 of small volume
  2. >5 episodes of >1 coffee spoon
  3. >5 episodes of half of the feedings in < half of the feedings
  4. Continuous regurgitations of small volumes >30 min after each feeding
  5. Regurgitation of half to complete volume of a feeding in at least half of the feedings
  6. Regurgitation of the 'complete feeding' after each feeding

The mean of score during 3 days is considered.

from 0 to 6 months
Number of wake up per night
Prazo: from 0 to 6 months
Evaluation during 3 consecutive days every month.
from 0 to 6 months
Total sleep time per day
Prazo: from 0 to 6 months
Time in hours. Evaluation during 3 consecutive days every month.
from 0 to 6 months
Plasma amino acid profile
Prazo: between 3rd and 4th month
Methods : Liquid Chromatography and Tandem Mass Spectrometry (LC / MS / MS) List of amino acids : Taurine, Aspartic acid, Threonine, Serine, Asparagine, Glutamine acid, Glutamine, Glycine, Alanine, Citrulline, Valine, Cystine, Methionine, Isoleucine, Leucine, Tyrosine, Phenylalanine, Beta aminoisobutyric acid, Ornithine, 1-Methyl-Histidine, Histidine, Lysine, 3-methyl-Histidine, Arginine, Hydroxyproline, Proline
between 3rd and 4th month
Metabolomic analysis from plasma and urine samples
Prazo: between 3rd and 4th month

Non-targeted analysis : evaluation of all small molecules in biological system, such as amino acids, sugars, alcohols, sugar phosphates, amines, fatty acids, polar lipids, hormones and vitamins, as well as specialized metabolites, such as phenolic compounds, flavonoids, monoterpenes, sesquiterpenes, polyketides, alkaloids, including xenobiotics.

Methods : Liquid Chromatography and Mass Spectrometry (LC / MS)

between 3rd and 4th month

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

30 de outubro de 2018

Conclusão Primária (Real)

30 de julho de 2020

Conclusão do estudo (Real)

30 de dezembro de 2021

Datas de inscrição no estudo

Enviado pela primeira vez

3 de dezembro de 2018

Enviado pela primeira vez que atendeu aos critérios de CQ

30 de abril de 2019

Primeira postagem (Real)

3 de maio de 2019

Atualizações de registro de estudo

Última Atualização Postada (Real)

27 de abril de 2022

Última atualização enviada que atendeu aos critérios de controle de qualidade

20 de abril de 2022

Última verificação

1 de abril de 2022

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 2018-A00732-53

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Ensaios clínicos em Desenvolvimento infantil

Ensaios clínicos em Breastfeeding

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