Non-invasive Continuous Cardiac Output Monitoring in Preterm Infants Study
Recruiting
Observational Study
Cardiac Output, Low
Cardiac Output, High
Blood Pressure
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 1 Hour – 40 Weeks
- Sex
- Any
- Study type
- Observational
- Participants needed
- 148 (estimated)
- Sponsor
- Imperial College Healthcare NHS Trust · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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 neonat…
Contacts
Sundar Sathiyamurthy Imperial College Healthcare NHS Trust
02033137308
CONTACT