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

2022년 4월 20일 업데이트: 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.

연구 개요

연구 유형

중재적

등록 (실제)

100

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

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

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

1일 (어린이)

건강한 자원 봉사자를 받아들입니다

예

연구 대상 성별

모두

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 다른
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 더블

무기와 개입

참가자 그룹 / 팔
개입 / 치료
위약 비교기: 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
활성 비교기: 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
활성 비교기: 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

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Evolution of growth of infants
기간: from 0 to 6 months
Weight in kilograms
from 0 to 6 months

2차 결과 측정

결과 측정
측정값 설명
기간
Height evolution of infants
기간: from 0 to 6 months
data in centimeters
from 0 to 6 months
BMI evolution of infants
기간: from 0 to 6 months
data in kg/m²
from 0 to 6 months
Head circumference evolution of infants
기간: from 0 to 6 months
data in centimeters
from 0 to 6 months
Number of colic per day
기간: from 0 to 6 months
Evaluation during 3 consecutives days every month.
from 0 to 6 months
Consistency of stool
기간: 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
기간: 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
기간: from 0 to 6 months
Evaluation during 3 consecutive days every month.
from 0 to 6 months
Total sleep time per day
기간: from 0 to 6 months
Time in hours. Evaluation during 3 consecutive days every month.
from 0 to 6 months
Plasma amino acid profile
기간: 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
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2018년 10월 30일

기본 완료 (실제)

2020년 7월 30일

연구 완료 (실제)

2021년 12월 30일

연구 등록 날짜

최초 제출

2018년 12월 3일

QC 기준을 충족하는 최초 제출

2019년 4월 30일

처음 게시됨 (실제)

2019년 5월 3일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2022년 4월 27일

QC 기준을 충족하는 마지막 업데이트 제출

2022년 4월 20일

마지막으로 확인됨

2022년 4월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 2018-A00732-53

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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