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What is the Future of Vulnerable New-borns

What is the Future of Vulnerable New-borns

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04021654
Acronym
DNNV
Enrollment
257
Registered
2019-07-16
Start date
2018-09-01
Completion date
2020-09-01
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preterm Birth

Keywords

Preterm birth; growth; neonatology; Pregnancy; Delivery

Brief summary

The aim of this data base is to know exactly the future of a vulnerable newborns cared in Pontoise Hospital (In the neonatology service) and compare the information with the national data of preterm birth.

Detailed description

The aim of this data base is to know exactly the future of a vulnerable newborns cared in Pontoise Hospital (In the neonatology service), it means, newborns who are in these following risk categories: * Birth before 33 weeks of amenorrhea * Birth between 33 and 36 weeks of amenorrhea and fetal growth retardation lower to the 3rd for the gestation age * Perinatal anoxic-ischemia * Other children whose birth, perinatal history or the existence of a pathology classified them in a category at risk of developmental psychomotor disorders, the co-twin of a child of the preceding groups. * A regular follow-up is made in Pontoise hospital till the age of 7 to 8 year sold. It tries to screen growth anomalies (neuromotor, sensorial, behavioral, and cognitive or growth development) or health status. The data collect allow us to monitor these parameters and do a statistical study with them. These information may be used to inform the parents about the future of the premature children cared at Pontoise. They also may be used to compare these children's future with the national data (EPIPAGE 2)

Interventions

PROCEDUREData collection

Data collection of growth, neuromotor, sensorial, behavioral, and cognitive development.

Sponsors

Hôpital NOVO
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Hours to 5 Years
Healthy volunteers
No

Inclusion criteria

* Birth before 33 weeks of amenorrhea * Birth between 33 and 36 weeks of amenorrhea and fetal growth retardation lower to the 3rd percentile for the gestational age. * Perinatal anoxic-ischemia Other children whose birth, perinatal history or the existence of a pathology classifies them in a category at risk of developmental psychomotor disorders, the co-twin of a child of the preceding groups.

Exclusion criteria

* Children born in normal conditions.

Design outcomes

Primary

MeasureTime frameDescription
The pregnancy issues rate2 yearsMeasure the rate of issues that occur during the pregnancy.
Delivrey issues rate2 yearsMeasurement of the rate of issues that occur during the delivery.
% of preterm children with a failure to thrive.2 yearsMeasurement of the % of children with a failure to thrive.

Secondary

MeasureTime frameDescription
Number of diseases in the children family health history.2 yearsCensus of all diseases that may be in the children family health history

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026