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Not Yet RecruitingNANCT06683677

High Flow Nasal Cannula for Stabilization of Extremely Premature Infants

A prospective observational study evaluates the safety and efficacy of using High-Flow Nasal Cannula to stabilize extremely preterm infants immediately after birth. Following placental transfusion, hi...

Lead sponsor: Charles University, Czech Republic•1 locations•View source on ClinicalTrials.gov

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Contacts

Klára Jonáš

CONTACT

00420602504067 klara.jonas@vfn.cz

Richard Plavka

CONTACT

Richard.Plavka@vfn.cz

Sponsors

Lead Sponsor

Charles University, Czech Republic

Age

All ages

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Preterm infants born between 25+0 and 27+6 gestational weeks
•Weight above 500 grams

Exclusion Criteria

•Previable rupture of membranes,
•Congenital malformations previable
•Acute intrauterine hypoxia.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: November 14, 2024Terms

Trial snapshot

StatusNOT_YET_RECRUITING

PhaseNA

Enrollment60

Start dateDec 2024

Last updatedNov 14, 2024

Condition

Premature Infant Ventilation Therapy High Flow Nasal Canula

Locations shown

General University Hospital Prague

Prague, Prague

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: November 14, 2024Data synced to Clareo: May 10, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions