About: Acute Bronchodilator Effect of Inhaled Albuterol Sulfate and Ipratropium Bromide in Patients With Stable COPD

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About: Acute Bronchodilator Effect of Inhaled Albuterol Sulfate and Ipratropium Bromide in Patients With Stable COPD Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

clinical trial

Attributes	Values
rdf:type	Item
description	clinical trial (en) ensayu clínicu (ast) klinisch onderzoek (nl) клінічне випробування (uk) կլինիկական փորձարկում (hy)
rdfs:label	Acute Bronchodilator Effect of Inhaled Albuterol Sulfate and Ipratropium Bromide in Patients With Stable COPD (en)
skos:prefLabel	Acute Bronchodilator Effect of Inhaled Albuterol Sulfate and Ipratropium Bromide in Patients With Stable COPD (en)
name	Acute Bronchodilator Effect of Inhaled Albuterol Sulfate and Ipratropium Bromide in Patients With Stable COPD (en)
title	wds:Q62811303-C607BB1D-2CDA-4F49-96F0-27B8B7C2A859
title	A Single Center Study to Measure the Bronchodilator Effect of Albuterol Sulfate or Albuterol Sulfate/Ipratropium Bromide Using the Pneuma Respiratory Inhaler and the ProAir HFA Inhaler in Stable COPD Patients (en)
end time	wds:Q62811303-41516242-F20C-476F-9225-B59E15E2A42C
end time	2017-04-28 00:00:00Z (xsd:dateTime)
instance of	wds:Q62811303-F617E419-11A0-422E-99AE-A23CC8940EDA
instance of	clinical trial
start time	wds:Q62811303-50564627-D6A4-4159-82ED-E0E708789908
start time	2016-12-27 00:00:00Z (xsd:dateTime)
country	wds:Q62811303-6F0A3877-1431-4C79-82AD-D6E271C2DBC1
country	United States of America
research intervention	wds:Q62811303-1032F529-9095-4BD1-AE71-C8C08027B0A8 wds:Q62811303-D7A8909F-5C0A-4F5A-9FD3-5E27359B6EE7 wds:Q62811303-F9137ED6-BAE2-4CDE-872B-65F33C572E2B
research intervention	ipratropium bromide/salbutamol bromide albuterol / ipratropium
minimum age	wds:Q62811303-6AEAC22D-713D-4FC5-8B86-7329BA5B9B3E
minimum age	40 (xsd:decimal)
number of participants	wds:Q62811303-CEC9AEB0-956C-41F8-900C-37008666117E
number of participants	46 (xsd:decimal)
maximum age	wds:Q62811303-9153C344-F2CF-4B74-A0C0-236E0B4068E2
maximum age	80 (xsd:decimal)
study type	wds:Q62811303-91D94F8C-2C74-40C6-BDAB-B13CBADA5D8C
study type	interventional study
ClinicalTrials.gov ID	wds:Q62811303-0C4891C1-CA12-4E27-BE68-F287843C4452
ClinicalTrials.gov ID	NCT03480997
clinical trial phase	wds:Q62811303-4317F672-93C9-4909-8FE1-ADF2611373BA
clinical trial phase	phase I clinical trial
research subject recruitment status	wds:Q62811303-33300897-DEEF-4472-BE3C-3243423EE2FB
research subject recruitment status	completed
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q62811303

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