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USCOM Parameters in Preterm Infants: Reference Ranges

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Fondazione IRCCS San Gerardo dei Tintori

Status

Enrolling

Conditions

Very Low Birth Weight Infant
Very Preterm Maturity of Infant

Treatments

Diagnostic Test: Hemodynamic measurements by USCOM

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this observational study is to learn about the feasibility of hemodynamic measurement by the UltraSonic Cardiac Output Monitor (USCOM) in very preterm or very-low-birth-weight infants. The main questions it aims to answer are: 1) establishing reference ranges for USCOM parameters in this specific population, 2) assessing the effect of patients' characteristics and other possible confounders on USCOM parameters, and 3) evaluating the short-term repeatability of the measurement. Participants will receive USCOM measurements on 3, 7, and 14 postnatal days.

Enrollment

80 estimated patients

Sex

All

Ages

2 to 16 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • gestational age at birth below 32 weeks and/or
  • birth weight (BW) below 1500 g

Exclusion criteria

  • congenital heart diseases,
  • hemodynamic instability requiring drugs that affect hemodynamics (e.g., inotropes)

Trial contacts and locations

1

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Central trial contact

Emanuela Zannin, PhD; Daniela Doni, MD

Data sourced from clinicaltrials.gov

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