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NCT00790166: CIA-6

Effects of nCPAP With and Without Humidification on: Inspiratory Temperature, Humidity, Saccharine Transit Time, Nasal Lavage and in Vitro Mucus Properties in Patients With Obstructive Sleep Apnea

Terminated NA Last updated 25 April 2018
What this trial tests

NA trial testing CPAP + ThermoSmart™ humidity in Obstructive Sleep Apnea in 4 participants. Terminated before completion.

Timeline
1 October 2008
Primary endpoint
24 June 2009
24 June 2009

Quick facts

Lead sponsorFisher and Paykel Healthcare
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposetreatment
Enrollment4
Start date1 October 2008
Primary completion24 June 2009
Estimated completion24 June 2009
Sites1 location across Brazil

Drugs / interventions tested

Conditions studied

Sponsor

Fisher and Paykel Healthcare — full company profile →

Who can join

18 and older, any sex, with Obstructive Sleep Apnea. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

That the level of humidification delivered to patients during CPAP treatment will alter the subjects mucociliary clearance rate and related mucus properties.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Obstructive Sleep Apnea

Currently open trials in the same condition.

Other Fisher and Paykel Healthcare 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/NCT00790166.

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