Actively Recruiting

Phase Not Applicable
Age: 2Weeks +
All Genders
NCT06207994

PRICO: OPTI Target Range

Led by Czech Technical University in Prague · Updated on 2025-03-25

10

Participants Needed

1

Research Sites

79 weeks

Total Duration

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Sponsors

C

Czech Technical University in Prague

Lead Sponsor

U

University Hospital, Motol

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of the study is to determine if a narrower SpO2 Target Range setting automated control of FiO2 (A-FiO2) is more effective than a wider SpO2 Target Range

CONDITIONS

Official Title

PRICO: OPTI Target Range

Who Can Participate

Age: 2Weeks +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Infants with very low birth weight on respiratory support and oxygen after 2 weeks of age in the NICU
  • Informed consent obtained
Not Eligible

You will not qualify if you...

  • Informed consent not obtained
  • Automated FiO2 control recording device not available

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Motol University Hospital

Prague, Czechia, 15500

Actively Recruiting

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Research Team

J

Jakub Rafl, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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