MedTrace Logo

USCOM Parameters in Preterm Infants: Reference Ranges

NCT05961657 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2023-07-27

No results posted yet for this study

Summary

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.

Conditions

  • Very Low Birth Weight Infant
  • Very Preterm Maturity of Infant

Interventions

DIAGNOSTIC_TEST

Hemodynamic measurements by USCOM

We will measure cardiac output, cardiac index, and systemic vascular resistance index on 3, 7, and 14 postnatal days using the UltraSonic Cardiac Output Monitor.

Sponsors & Collaborators

  • Fondazione IRCCS San Gerardo dei Tintori

    lead OTHER

Principal Investigators

  • Daniela Doni, MD · Fondazione IRCCS San Gerardo dei Tintori

Eligibility

Min Age
2 Days
Max Age
16 Days
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-06
Primary Completion
2023-08-09
Completion
2023-09-01

Countries

  • Italy

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05961657 on ClinicalTrials.gov