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Optimal Growth of Preterm Infants With Growth Restriction (OPTIGROW)

Primary Purpose

Growth Failure, Adiposity, Diabetes

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
SGA-enhanced nutrients
IUGR-enhanced nutrients
SGA-standard nutrients
IUGR-standard nutrients
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Growth Failure focused on measuring preterm infants, SGA infants, IUGR infants, growth, body composition, metabolomics, microbiome, adiposity markers, metabolic programming, neurodevelopmental outcome

Eligibility Criteria

undefined - 42 Weeks (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Preterm infants with a birth weight <1500g and birth weight <10th percentile.
  • Weight at term <10th percentile
  • Informed consent

Exclusion Criteria:

  • Genetic or metabolic diseases with the primary effect on growth
  • Necrotizing enterocolitis
  • Intraventricular hemorrhage (IVH) >Grade II
  • Periventricular leukomalacia (PVL) Stage III
  • Genetic or metabolic disorders
  • Bronchopulmonary dysplasia

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Active Comparator

    Other

    Active Comparator

    Other

    Arm Label

    SGA-enhanced nutrients

    SGA-standard nutrients

    IUGR-enhanced nutrients

    IUGR-standard nutrients

    Arm Description

    Infants will receive fortified breast milk (>50% meals/d fortified, 1,4 g protein, 85 kcal/100ml, FM85, Nestle ®) or post discharge formula (2g protein; 73-75 kcal/100ml; Aptamil PDF, Milupa® or Beba F Nestle® ) between discharge and 52nd week of gestation (three months after term)

    Infants will receive unfortified breast milk (65-70kcal/100ml) or starter formula (1,2- 1,3g protein, 66 kcal/100ml Beba Pre Pro Start, Nestle® or Aptamil Pre, Milupa ®) between discharge and 52nd week of gestation (three months after term).

    Infants will receive fortified breast milk (>50% meals/d fortified, 1,4 g protein, 85 kcal/100ml, FM85, Nestle ®) or post discharge formula (2g protein; 73-75 kcal/100ml; Aptamil PDF, Milupa® or Beba F Nestle® ) between discharge and 52nd week of gestation (three months after term

    Infants will receive unfortified breast milk (65-70kcal/100ml) or starter formula (1,2- 1,3g protein, 66 kcal/100ml Beba Pre Pro Start, Nestle® or Aptamil Pre, Milupa ®) between discharge and 52nd week of gestation (three months after term).

    Outcomes

    Primary Outcome Measures

    Fat Free Mass
    Fat free mass measured by body plethysmography

    Secondary Outcome Measures

    anthropometry-length
    length in cm
    anthropometry-weight
    weight in grams
    anthropometry-HC
    head circumference in cm
    anthropometry-z-score
    z-scores
    parameters of metabolic programming- IGF1
    IGF-1in ng/ml
    parameters of metabolic programming-IGF3
    IGF-3 in ng/ml
    parameters of metabolic programming-IGF-BP
    IGF-BP in ng/ml
    parameters of metabolic programming-Leptin
    Leptin in ng/ml
    parameters of metabolic programming-Adiponectin
    Adiponectin in mcg/ml
    neurodevelopmental outcome
    Bayley scales
    metabolomics
    Metabolomic analysis will determine around 200 metabolites covering polar lipids (SOFIA), acylcarnitines (CARN), non-esterified fatty acids (NEFA) and amino acids (AA). Data will be acquired according to retention time and mass transition on triple quadrupole mass spectrometer, controlled by Analyst. All metabolite concentrations are reported in µmol/L
    stool microbiome
    macronutrients in breastmilk-fat
    Fat will be analysed by modified Mojonnierether extraction (g/100ml)
    macronutrients in breastmilk-Lactose
    Lactose will be determined by Lactose analysis method: LC-MS/MS (g/100ml)
    macronutrients in breastmilk-protein
    Protein will be determined by elemental analysis (g/100ml)

    Full Information

    First Posted
    December 5, 2016
    Last Updated
    March 19, 2019
    Sponsor
    Medical University of Vienna
    Collaborators
    Medical University of Graz, Ludwig-Maximilians - University of Munich, University Hospital Tuebingen, University of Erlangen-Nürnberg Medical School, University of Milan, Poznan University of Medical Sciences, Lund University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02999945
    Brief Title
    Optimal Growth of Preterm Infants With Growth Restriction
    Acronym
    OPTIGROW
    Official Title
    Body Composition, Metabolic Programming and Long Term Outcome of Growth Restricted Preterm Infants Under Different Nutritional Management A Prospective Randomized Controlled Multicenter Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2019
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    no funding
    Study Start Date
    March 2019 (Anticipated)
    Primary Completion Date
    January 2020 (Anticipated)
    Study Completion Date
    January 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Medical University of Vienna
    Collaborators
    Medical University of Graz, Ludwig-Maximilians - University of Munich, University Hospital Tuebingen, University of Erlangen-Nürnberg Medical School, University of Milan, Poznan University of Medical Sciences, Lund University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    In this prospective randomized controlled multi center trial the investigators stratify "Very Low Birthweight " (VLBW)-infants with growth retardation in small for gestational age (SGA) or intrauterine growth restricted (IUGR) - infants and aim to investigate the impact of a nutritional management with enhanced nutrients from discharge up to the 52nd week of postconceptional age on growth, body composition, metabolic programming, metabolomics, microbiome and long term neurodevelopmental outcome. In this study, the investigators will evaluate the difference in metabolic profiles of SGA and IUGR preterm infants. The investigators will further longitudinally assess, how different nutritional interventions affect the altered pathways in the first year of life and identify, in combination with data available from metabolic markers, microbiome and breast milk analysis, potential pathways resulting in increased disease risk later in life.
    Detailed Description
    Prematurity is the leading cause for mortality and morbidity in newborns with very low birth weight (VLBW) infants (< 1500g birth weight) at highest risk. Ten to thirty percent of VLBW infants are also born too small for their gestational age defined by a birth weight below the 10th percentile. In daily neonatal intensive care, consequential long term-follow up and most studies all growth restricted premature infants are treated the same, importantly this includes the nutritional management after birth. However, different groups of patients with different causal pathologies are subsumed under the definition growth restriction or born too small. One group of growth restricted patients refers to the infants born constitutionally small or small for gestational age (SGA). The other group refers to infants with an intrauterine growth restriction (IUGR) caused by a complex antenatal pathology. Consequently, the nutritional management after birth is very important to minimize the potential risk for developing obesity, diabetes and cardiovascular diseases later in life and to achieve optimal growth. So far we do not consider the different underlying pathomechanisms of growth restriction in our nutritional concepts for preterm infants and therefore cause long-term consequences. The European society of pediatric gastroenterology, hematology and nutrition (ESPGHAN) recommends to feed enhanced nutrients up to 52nd week of gestation in all growth restricted preterm infants- regardless if they are SGA or IUGR premature. Actually, reliable data guaranteeing that the recommended "enhanced nutrients strategy" providing extra nutrients up to 52 weeks for SGA and IUGR infants is safe and effective for both groups in terms of long-term growth and metabolic programming are lacking. A total of 348 preterm infants born and discharged below the 10th percentile at term will be included in the study and stratified according to SGA or IUGR by a combination of antenatal ultrasound parameters and growth parameters (including 10% screening failures and 20% drop out. Furthermore IUGR and SGA growth restricted preterm infants will be stratified according to breastfeeding or formula feeding and randomized in one of the following groups: Standard nutrients group (breastfeeding or starter formula) or Enhanced nutrients group (fortified breast milk or post-discharge formula. Body composition measurements will be performed by air displacement plethysmography - a non-invasive method. Anthropometric measurements will be performed by measuring weight, height and head circumference. Furthermore, parameters of metabolic programming, metabolomics, the stool microbiome and neurodevelopmental outcome will be determined. Additionally, the stool microbiome will be characterized from infant stool samples and compared between the two groups. After an interventional period of three months infants will be followed up until 2 years of age.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Growth Failure, Adiposity, Diabetes, Neurologic Deficits
    Keywords
    preterm infants, SGA infants, IUGR infants, growth, body composition, metabolomics, microbiome, adiposity markers, metabolic programming, neurodevelopmental outcome

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    SGA-enhanced nutrients
    Arm Type
    Active Comparator
    Arm Description
    Infants will receive fortified breast milk (>50% meals/d fortified, 1,4 g protein, 85 kcal/100ml, FM85, Nestle ®) or post discharge formula (2g protein; 73-75 kcal/100ml; Aptamil PDF, Milupa® or Beba F Nestle® ) between discharge and 52nd week of gestation (three months after term)
    Arm Title
    SGA-standard nutrients
    Arm Type
    Other
    Arm Description
    Infants will receive unfortified breast milk (65-70kcal/100ml) or starter formula (1,2- 1,3g protein, 66 kcal/100ml Beba Pre Pro Start, Nestle® or Aptamil Pre, Milupa ®) between discharge and 52nd week of gestation (three months after term).
    Arm Title
    IUGR-enhanced nutrients
    Arm Type
    Active Comparator
    Arm Description
    Infants will receive fortified breast milk (>50% meals/d fortified, 1,4 g protein, 85 kcal/100ml, FM85, Nestle ®) or post discharge formula (2g protein; 73-75 kcal/100ml; Aptamil PDF, Milupa® or Beba F Nestle® ) between discharge and 52nd week of gestation (three months after term
    Arm Title
    IUGR-standard nutrients
    Arm Type
    Other
    Arm Description
    Infants will receive unfortified breast milk (65-70kcal/100ml) or starter formula (1,2- 1,3g protein, 66 kcal/100ml Beba Pre Pro Start, Nestle® or Aptamil Pre, Milupa ®) between discharge and 52nd week of gestation (three months after term).
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    SGA-enhanced nutrients
    Intervention Description
    Infants will receive fortified breast milk (>50% meals/d fortified, 1,4 g protein, 85 kcal/100ml, FM85, Nestle ®) or post discharge formula (2g protein; 73-75 kcal/100ml; Aptamil PDF, Milupa® or Beba F Nestle® ) between discharge and 52nd week of gestation (three months after term
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    IUGR-enhanced nutrients
    Intervention Description
    Infants will receive fortified breast milk (>50% meals/d fortified, 1,4 g protein, 85 kcal/100ml, FM85, Nestle ®) or post discharge formula (2g protein; 73-75 kcal/100ml; Aptamil PDF, Milupa® or Beba F Nestle® ) between discharge and 52nd week of gestation (three months after term
    Intervention Type
    Other
    Intervention Name(s)
    SGA-standard nutrients
    Intervention Description
    Infants will receive unfortified breast milk (65-70kcal/100ml) or starter formula (1,2- 1,3g protein, 66 kcal/100ml Beba Pre Pro Start, Nestle® or Aptamil Pre, Milupa ®) between discharge and 52nd week of gestation (three months after term)
    Intervention Type
    Other
    Intervention Name(s)
    IUGR-standard nutrients
    Intervention Description
    Infants will receive unfortified breast milk (65-70kcal/100ml) or starter formula (1,2- 1,3g protein, 66 kcal/100ml Beba Pre Pro Start, Nestle® or Aptamil Pre, Milupa ®) between discharge and 52nd week of gestation (three months after term)
    Primary Outcome Measure Information:
    Title
    Fat Free Mass
    Description
    Fat free mass measured by body plethysmography
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    anthropometry-length
    Description
    length in cm
    Time Frame
    24 months
    Title
    anthropometry-weight
    Description
    weight in grams
    Time Frame
    24 months
    Title
    anthropometry-HC
    Description
    head circumference in cm
    Time Frame
    24 months
    Title
    anthropometry-z-score
    Description
    z-scores
    Time Frame
    24 months
    Title
    parameters of metabolic programming- IGF1
    Description
    IGF-1in ng/ml
    Time Frame
    12 months
    Title
    parameters of metabolic programming-IGF3
    Description
    IGF-3 in ng/ml
    Time Frame
    12 months
    Title
    parameters of metabolic programming-IGF-BP
    Description
    IGF-BP in ng/ml
    Time Frame
    12 months
    Title
    parameters of metabolic programming-Leptin
    Description
    Leptin in ng/ml
    Time Frame
    12 months
    Title
    parameters of metabolic programming-Adiponectin
    Description
    Adiponectin in mcg/ml
    Time Frame
    12 months
    Title
    neurodevelopmental outcome
    Description
    Bayley scales
    Time Frame
    24months
    Title
    metabolomics
    Description
    Metabolomic analysis will determine around 200 metabolites covering polar lipids (SOFIA), acylcarnitines (CARN), non-esterified fatty acids (NEFA) and amino acids (AA). Data will be acquired according to retention time and mass transition on triple quadrupole mass spectrometer, controlled by Analyst. All metabolite concentrations are reported in µmol/L
    Time Frame
    12 months
    Title
    stool microbiome
    Time Frame
    24 months
    Title
    macronutrients in breastmilk-fat
    Description
    Fat will be analysed by modified Mojonnierether extraction (g/100ml)
    Time Frame
    6 months
    Title
    macronutrients in breastmilk-Lactose
    Description
    Lactose will be determined by Lactose analysis method: LC-MS/MS (g/100ml)
    Time Frame
    6 months
    Title
    macronutrients in breastmilk-protein
    Description
    Protein will be determined by elemental analysis (g/100ml)
    Time Frame
    6 months

    10. Eligibility

    Sex
    All
    Maximum Age & Unit of Time
    42 Weeks
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Preterm infants with a birth weight <1500g and birth weight <10th percentile. Weight at term <10th percentile Informed consent Exclusion Criteria: Genetic or metabolic diseases with the primary effect on growth Necrotizing enterocolitis Intraventricular hemorrhage (IVH) >Grade II Periventricular leukomalacia (PVL) Stage III Genetic or metabolic disorders Bronchopulmonary dysplasia
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Nadja Haiden, MD
    Organizational Affiliation
    MUW
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Optimal Growth of Preterm Infants With Growth Restriction

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