About: Onset of Action of Advair Hydrofluoroalkane (HFA) 115/21 in Comparison to Symbicort Pressurised Metered-Dose Inhalers (pMDI) 160/4.5 Measured by Impulse Oscillometry (IOS)

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About: Onset of Action of Advair Hydrofluoroalkane (HFA) 115/21 in Comparison to Symbicort Pressurised Metered-Dose Inhalers (pMDI) 160/4.5 Measured by Impulse Oscillometry (IOS) Goto Sponge NotDistinct Permalink

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clinical trial

Attributes	Values
rdf:type	Item
description	clinical trial (en) ensayo clínico (es) ensayu clínicu (ast) klinisch onderzoek (nl) клінічне випробування (uk)
rdfs:label	Onset of Action of Advair Hydrofluoroalkane (HFA) 115/21 in Comparison to Symbicort Pressurised Metered-Dose Inhalers (pMDI) 160/4.5 Measured by Impulse Oscillometry (IOS) (en)
skos:prefLabel	Onset of Action of Advair Hydrofluoroalkane (HFA) 115/21 in Comparison to Symbicort Pressurised Metered-Dose Inhalers (pMDI) 160/4.5 Measured by Impulse Oscillometry (IOS) (en)
name	Onset of Action of Advair Hydrofluoroalkane (HFA) 115/21 in Comparison to Symbicort Pressurised Metered-Dose Inhalers (pMDI) 160/4.5 Measured by Impulse Oscillometry (IOS) (en)
title	wds:Q61980871-6AF671AF-169E-40A7-968C-EA089F4887DC
title	Onset of Action of Advair HFA 115/21 in Comparison to Symbicort pMDI 160/4.5 Measured by Impulse Oscillometry, IOS. (en)
end time	wds:Q61980871-1B90BF29-C345-4759-B0D8-CB74697FCF8C
end time	2009-09-01 00:00:00Z (xsd:dateTime)
instance of	wds:Q61980871-FD07817A-C09B-4FEC-8F6E-44672061B3D0
instance of	clinical trial
start time	wds:Q61980871-BC8F416E-1CCA-47EC-BB4E-3FCA1AF62712
start time	2008-09-01 00:00:00Z (xsd:dateTime)
country	wds:Q61980871-F75EA9E5-26CF-4978-BB2E-BB9DC0A8F8E3
country	United States of America
main subject	wds:Q61980871-516D0365-F113-4230-9578-52514DBEF80A
main subject	Impulse oscillometry in COPD: Identification of measurements related to airway obstruction, airway conductance and lung volumes
research intervention	wds:Q61980871-E6EE7C92-191A-43DA-A519-26173E5F7117
research intervention	formoterol fumarate
minimum age	wds:Q61980871-2FB570B3-46AB-4F27-8130-BD459034A15E
minimum age	12 (xsd:decimal)
number of participants	wds:Q61980871-EEEF451D-0924-4647-B87C-E1F4C9C42CE6
number of participants	30 (xsd:decimal)
maximum age	wds:Q61980871-C8B40F21-1FE8-412A-B0A5-526E1175EAC1
maximum age	45 (xsd:decimal)
study type	wds:Q61980871-C02DA8BC-F4F9-4BCB-B166-8F518DBD5E0C
study type	interventional study
ClinicalTrials.gov ID	wds:Q61980871-88DAB5C5-BD53-4327-AED0-3F13A6B0AC23
ClinicalTrials.gov ID	NCT00867737
clinical trial phase	wds:Q61980871-0C232D3B-95B9-48F4-9B8F-22079F142131
clinical trial phase	phase IV clinical trial
research subject recruitment status	wds:Q61980871-E8C100BB-51B7-4269-9A87-9F4886E288BA
research subject recruitment status	unknown
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q61980871

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