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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01450436
Other study ID # PROG/11/80
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 2011
Est. completion date October 2014

Study information

Verified date February 2020
Source Nantes University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Neonatal nutritional management consists in reproducing miming uteri growth kinetic. Since the seventies, NICU (Neonatal Intensive Care Unit) strategy consists in a high proteidic input (apport) supposed to allow optimal neurodevelopment. However, nutritional practices and strategies have significantly evolved during these last years, influenced by Baker nutritional imprinting concept (2002). Actually, neonatal high proteidic exposition could perturb metabolism and hormonal systems of newborns conducting to a reinforcement of obesity and cardio-vascular pathology prevalence in this target population at adulthood. In this context many studies emerged since 2000 and try to assess the trade-off between neurodevelopment and growth under nutrition conditions. EPIPOD try to focus the link between heterogenous proteic input dispensed in our NICU (described by tercil methods on population) and fat mass phenotype variations at discharge (described by tercil methods); and its consequences on neurodevelopmental growth. Understanding how particular nutritional exposition could determine "fatty" phenotype and impact neurodevelopment is clearly our main goal.


Recruitment information / eligibility

Status Completed
Enrollment 270
Est. completion date October 2014
Est. primary completion date October 2014
Accepts healthy volunteers No
Gender All
Age group 25 Weeks to 35 Weeks
Eligibility Inclusion Criteria:

- Preterm newborns (< 35 weeks gestation).

- Final clinical discharge (No transfer)

- Oral Parental consent.

- Nantes NICU Neonatal management in the first 5 days of life

Exclusion Criteria:

- Congenital pathology inconsistent with PEAPOD investigation (Beckwith-Wiedemann syndrome, lipodystrophia with abnormal constitutional fat mass level).

- Pathology inducing neurodevelopment troubles.

- Transfer in an other hospital before discharge

- Hemodynamic or cardiovascular instability requiring continuous monitoring or perfusion, incompatible with PEAPOD measurement

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Peapod assessment
EPIPOD consists in a Non-Interventional Research according to French regulations. Actually, Peapod examination at discharge takes part of current clinical practice and patient management in Nantes Neonatal Intensive Care Unit since 2008. After checking inclusion and non-inclusion criteria and obtaining oral informed consent from newborn legal authority or parents, PEAPOD assessment was leaded in the last week of hospitalization. Consisting in 2 repeated measurement, body composition estimation was completed by clinical and demographic data as neonatal nutrition (Parenteral nutrition pattern at Day 5, 10 and 21, and ASQ/BLR Neurodevelopmental assessment at 2 years old).

Locations

Country Name City State
France Nantes University Hospital Nantes

Sponsors (1)

Lead Sponsor Collaborator
Nantes University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fatty mass percentage at discharge by PEAPOD measurement After checking inclusion and non-inclusion criteria and obtaining oral informed consent from newborn legal authority or parents, PEAPOD assessment was leaded in the last week of hospitalization. Consisting in 2 repeated measurement, body composition estimation was completed by clinical and demographic data as neonatal nutrition (Parenteral nutrition pattern at Day 5, 10 and 21, and ASQ/BLR Neurodevelopmental assesmment at 2 years old). PEAPOD measurement will be done at newborns discharge, at an expected average of 6.4 weeks hospitalization
Primary Children neurological development at 2 years old evaluated by Ages and stages questionnaires (ASQ) ASQ/BLR Neurodevelopmental assesmment at 2 years old.
Secondary body composition of preterm infants at discharge and full term newborns at 3 days of life PEAPOD measurement will be done at newborns discharge, at an expected average of 6.4 weeks hospitalization
Secondary Relationship between body composition at discharge and that at 2 years PEAPOD measurement will be done at newborns discharge, at an expected average of 6.4 weeks hospitalization
Secondary Impact of fatty mass percentage at preterm newborns discharge on neurologic outcome assessed by a revised Brunet-Lezine test at 2 years. PEAPOD measurement will be done at newborns discharge, at an expected average of 6.4 weeks hospitalization
Secondary Preterm infants feeding behavior at 2 years At 2 years old
Secondary Factors (both intrinsic and nutritional) influencing body composition of preterm infants (<35 weeks gestation), at discharge factors influencing body composition report will be done at newborns discharge, at an expected average of 6.4 weeks hospitalization
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