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NCT04459429

Effect of Cannula Size on Oxygen Saturation During Nasal High Flow Therapy in Newborns

Completed NA Last updated 30 June 2021
What this trial tests

NA trial testing Change of cannula size in RDS - Infants in 25 participants. Completed in 24 December 2020.

Timeline
26 June 2020
Primary endpoint
24 December 2020
24 December 2020

Quick facts

Lead sponsorErebouni Medical Center
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment25
Start date26 June 2020
Primary completion24 December 2020
Estimated completion24 December 2020
Sites1 location across Armenia

Drugs / interventions tested

Conditions studied

Sponsor

Erebouni Medical Center

Who can join

Adults 1 Hour to 2 Days, any sex, with RDS - Infants or TTN. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Treatment with nasal high flow therapy (NHF) is an increasingly popular method of respiratory support in newborns. Safe and effective use of NHF requires selection of an appropriate nasal prong-to-nares ratio because leak can influence the delivered pressure. To the best of our knowledge, this is the first study to investigate the effect of using different NHF cannula size on peripheral oxygen saturation in newborns with respiratory distress.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Erebouni Medical Center trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04459429.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing