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Clinical Trials/NCT02863978
NCT02863978
Active, not recruiting
Not Applicable

Preliminary Study to the Conception of a Non-invasive Neonatal Monitoring System With Development of a Database

Rennes University Hospital6 sites in 1 country746 target enrollmentNovember 8, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Infant, Premature
Sponsor
Rennes University Hospital
Enrollment
746
Locations
6
Primary Endpoint
Number of newborns in neonatology unit
Status
Active, not recruiting
Last Updated
3 years ago

Overview

Brief Summary

Each year, 300 000 new borns are hospitalised in neonatology units in Europe. This period is very sensitive as newborns are exposed to a high risk of morbidity and mortality, with severe impact on neuro-developmental prognostic. The Rennes University Hospital was granted a specific funding from the European Union in the framework of the Horizon 2020 programme (Call PERSONALISING HEALTH AND CARE 2015-single-stage - Grant Agreement Number 689260) to develop the Digi-NewB project. This project aims to develop innovative non-invasive monitoring tools to support decision making in health. Such tools include a new generation of real time monitoring in neonatology using composite indices made of cardio-respiratory variables, movements, sounds, and clinical data. The Digi-NewB cohort aims to gather all physiological data relevant for the creation of the composite indices.

Detailed Description

The database will be used to answer the following specific objectives, with priority given to the two first ones (sepsis and maturation) : 1. Early diagnosis of sepsis for the following cases : Late onset sepsis of premature newborns, materno-fœtal sepsis, and newborn infection by chorioamnionitis 2. Cardio-respiratory and neurobehavioral maturation (movements, sleeping cycles) 3. Influence of environmental factors and developmental care on selected parameters 4. Influence on care organisation of the possibility to access videos and movement analyses by medical teams 5. Influence of glycemia on selected parameters 6. Influence of neurological lesions and broncho-pulmonary dysplasia on selected parameters 7. Indices correlation with medical images MRI (T1, T2, diffusion, Arterial Spin Labelling) from neonatal units and with health evaluated after 1 and 2 years with the Ages \& Stages Questionnaires (ASQ) 8. Evaluation of the acquisition system's user-friendliness

Registry
clinicaltrials.gov
Start Date
November 8, 2016
End Date
June 10, 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Rennes University Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Newborn hospitalised in the neonatology services of participating hospitals
  • One of the legal representatives gave its signed agreement to take part to the study
  • New born aged of less than 6 weeks in corrected term

Exclusion Criteria

  • No signed agreement from the legal representative

Outcomes

Primary Outcomes

Number of newborns in neonatology unit

Time Frame: Four years

Secondary Outcomes

  • Maturation(During the stay in neonatal unit, up to 10 weeks)
  • Influence of environment and developmental care(During the stay in neonatal unit, up to 10 weeks)
  • Glycemia(During the stay in neonatal unit, up to 10 weeks)
  • Medium term Prognosis(During the stay in neonatal unit, up to 10 weeks)
  • Infection/Sepsis(During the stay in neonatal unit, up to 10 weeks)
  • Care givers satisfaction(Each 6 months after setting up the acquisition system in the unit)
  • Impact on newborn's time of quiet sleep(At the end of the stay in neonatal unit, up to 10 weeks)
  • Prognosis evaluation(At the babies 1st and 2nd birthdays)
  • Cerebral Electrophysiology(During the stay in neonatal unit, up to 10 weeks)

Study Sites (6)

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