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NCT03411876: IPF/Oxymizer2

Effects of Oxymizer Pendant Cannula Versus Conventional Nasal Cannula During Endurance Shuttle Walk Tests in Hypoxemic Patients With Idiopathic Pulmonary Fibrosis

Completed NA Last updated 16 April 2020
What this trial tests

NA trial testing Oxymizer® pendant nasal cannula in Idiopathic Pulmonary Fibrosis in 22 participants. Completed in 15 January 2019.

Timeline
18 January 2018
Primary endpoint
15 January 2019
15 January 2019

Quick facts

Lead sponsorKlaus Kenn
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposetreatment
Enrollment22
Start date18 January 2018
Primary completion15 January 2019
Estimated completion15 January 2019
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Klaus Kenn

Who can join

Eligibility, any sex, with Idiopathic Pulmonary Fibrosis or Hypoxemia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Aim of this study is to investigate the effects of an Oxymizer pendant nasal cannula in hypoxemic patients with idiopathic pulmonary fibrosis during walking.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Acute effects of supplemental oxygen therapy using different nasal cannulas on walking capacity in patients with idiopathic pulmonary fibrosis: a randomised crossover trial.
    Schneeberger T, Leitl D, Gloeckl R, Jarosch I, et al · · 2020 · cited 1× · PMID 32832533 · DOI 10.1183/23120541.00197-2020

Verify or expand the search:

Other recruiting trials for Idiopathic Pulmonary Fibrosis

Currently open trials in the same condition.

Other Klaus Kenn trials

Trials by the same sponsor.

Verify against primary sources

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/NCT03411876.

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