RecruitingNCT04064177
Non-invasive Continuous Cardiac Output Monitoring in Preterm Infants Study
Sponsor
Imperial College Healthcare NHS Trust
Enrollment
148 participants
Start Date
Oct 24, 2019
Study Type
OBSERVATIONAL
Conditions
Summary
This is an observational study in newborn term and preterm infants. The study will validate if non-invasive continuous cardiac output monitoring is feasible in newborn infants, if normative values can be constructed and what is the effect of fluid boluses and inotropes on cardiac output and peripheral vascular resistance.
Eligibility
Min Age: 1 HourMax Age: 40 Weeks
Inclusion Criteria3
- Healthy term infants in postnatal ward (within the first 72 hours of age)
- Term and Preterm infants (including those with FGR) admitted to the neonatal unit
- Written informed parental consent (prospective for postnatal ward and retrospective for babies admitted to the neonatal units)
Exclusion Criteria4
- Antenatal or postnatal diagnosis of severe congenital anomaly
- Infants with no realistic chance of survival
- Infants who are >12 hours of age
- Infants with fragile skin not permitting skin probe placement
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Interventions
DEVICENICAS cardiac output monitor
Non-invasive continuous cardiac output monitoring device using total body bioimpedance.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT04064177
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