About: Efficacy and Safety of Hydrocodone Bitartrate (HYD) in Subjects With Moderate to Severe Chronic Low Back Pain

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About: Efficacy and Safety of Hydrocodone Bitartrate (HYD) in Subjects With Moderate to Severe Chronic Low Back Pain 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) ensayo clínico (es) ensayu clínicu (ast) klinisch onderzoek (nl) клінічне випробування (uk)
rdfs:label	Efficacy and Safety of Hydrocodone Bitartrate (HYD) in Subjects With Moderate to Severe Chronic Low Back Pain (en)
skos:prefLabel	Efficacy and Safety of Hydrocodone Bitartrate (HYD) in Subjects With Moderate to Severe Chronic Low Back Pain (en)
name	Efficacy and Safety of Hydrocodone Bitartrate (HYD) in Subjects With Moderate to Severe Chronic Low Back Pain (en)
title	wds:Q61967058-D77EF538-E752-4D7A-9F0D-E9AB32C990CB
title	A Multicenter, Randomized, Double-blind, Placebo-controlled Study With an Open-label Run-in to Assess the Efficacy and Safety of Hydrocodone Bitartrate (HYD) Tablets 20 to 120 mg Once-daily in Subjects With Moderate to Severe Chronic Low Back Pain (en)
end time	wds:Q61967058-E560D83B-E368-41CF-98A7-53AB7A77B94A
end time	2013-09-01 00:00:00Z (xsd:dateTime)
instance of	wds:Q61967058-1499079C-DE8A-4330-94E3-CFBF0FF86169
instance of	clinical trial
start time	wds:Q61967058-E8E94EA7-8CAD-4D15-BFF6-EC11B1B46FE5
start time	2011-10-01 00:00:00Z (xsd:dateTime)
country	wds:Q61967058-0EA1DD9B-BC29-4C52-9375-F186DA645CDC
country	United States of America
main subject	wds:Q61967058-A3AC94B2-31D9-4E27-8A39-3105DDD8CA01
main subject	pain
research site	wds:Q61967058-0FAFCA56-681D-4A6C-80AE-DD731421652E wds:Q61967058-1DC727B6-6A08-4AE5-8B7B-E821AAFEEB04 wds:Q61967058-2028F459-8911-4E18-9450-B9BF6813FCDC wds:Q61967058-62D70C32-612F-42A9-865E-41DB56311A49 wds:Q61967058-667C4751-92AC-4EC1-A54C-A9EE65279B22 wds:Q61967058-6BA57DB7-7C51-47BC-9FD0-6B4661E9590E wds:Q61967058-BC28A6C3-32B6-45E2-8EAF-981C1668627E wds:Q61967058-C32FB61D-649E-4470-A0AE-7B2C146D5C28 wds:Q61967058-E7DD2757-DCE1-47CA-9733-D4A3AC23AC05 wds:Q61967058-F2974DB3-F83A-477B-B852-D6258832BECA wds:Q61967058-F9C93FDD-466E-4752-B582-41312443DF10
research site	Northwest Clinical Research Center Avail Clinical Research Compass Research Drug Trials America Meridien Research Sundance Clinical Research Radiant Research (United States) Beacon Clinical Research Clinical Physiology Associates Quest Research Institute Medex
research intervention	wds:Q61967058-F43F03F9-5B70-4DED-A034-67FEDCAF58AC
research intervention	hydrocodone
minimum age	wds:Q61967058-F960BA8A-892F-4268-8A9A-448CC2B19995
minimum age	18 (xsd:decimal)
number of participants	wds:Q61967058-AE94BA1A-FEA6-4C06-AFD3-355ADC165EB9
number of participants	905 (xsd:decimal)
study type	wds:Q61967058-23C596C2-04DF-437A-9ED3-E2FD2769F096
study type	interventional study
ClinicalTrials.gov ID	wds:Q61967058-AF08A62E-04DA-4477-BA92-903283BC4C05
ClinicalTrials.gov ID	NCT01452529
clinical trial phase	wds:Q61967058-6F3BDD27-0809-4EC9-9EBA-0B9152B9E96D
clinical trial phase	phase III clinical trial
research subject recruitment status	wds:Q61967058-B8E75D04-BAFB-4334-9EC0-DAAC7E0F50F6
research subject recruitment status	completed
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q61967058

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