About: SWOG-9342 Chemotherapy in Treating Women Enrolled in the SWOG-8897 Clinical Trial

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About: SWOG-9342 Chemotherapy in Treating Women Enrolled in the SWOG-8897 Clinical Trial Goto Sponge Distinct 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)
rdfs:label	SWOG-9342 Chemotherapy in Treating Women Enrolled in the SWOG-8897 Clinical Trial (en) SWOG-9342 Chemotherapy in Treating Women Enrolled in the SWOG-8897 Clinical Trial (nl)
skos:prefLabel	SWOG-9342 Chemotherapy in Treating Women Enrolled in the SWOG-8897 Clinical Trial (en) SWOG-9342 Chemotherapy in Treating Women Enrolled in the SWOG-8897 Clinical Trial (nl)
name	SWOG-9342 Chemotherapy in Treating Women Enrolled in the SWOG-8897 Clinical Trial (en) SWOG-9342 Chemotherapy in Treating Women Enrolled in the SWOG-8897 Clinical Trial (nl)
title	wds:Q66038408-5E091256-1CED-44BF-B16D-52D108A66FBC
title	A STUDY OF THE LATE CARDIAC EFFECTS OF TWO DIFFERENT ADJUVANT CHEMOTHERAPY REGIMENTS IN WOMEN WITH NODE NEGATIVE BREAST CANCER TREATED ON SWOG-8897 (en)
end time	wds:Q66038408-359E50EB-4AE4-493A-9A09-6624CFF4ACA0
end time	2008-03-01 00:00:00Z (xsd:dateTime)
instance of	wds:Q66038408-E9402696-DA2C-4BEB-BC6F-32E34DDD9A12
instance of	clinical trial
start time	wds:Q66038408-5E4E761B-1552-40BA-90AC-A0AB147B5BAA
start time	1997-02-01 00:00:00Z (xsd:dateTime)
country	wds:Q66038408-49AD7270-E5FA-4ED1-9388-81593A639489
country	United States of America
research site	wds:Q66038408-211E4A45-C0E2-47D0-AC97-EF47E173DBC9 wds:Q66038408-23594674-D3B8-4E2E-B006-C1DC03DF954F wds:Q66038408-3486615F-D36D-46A1-A6E7-2A29A6F093F1 wds:Q66038408-4BAE34D3-26A8-48E7-B557-66C65829DC7C wds:Q66038408-5A86DA01-52F7-4D3E-BE82-194D38FF887A wds:Q66038408-5D8BADD1-410B-450D-8790-83EF916807E5 wds:Q66038408-602AB4CB-7FED-4A41-BF95-59213DB69E0E wds:Q66038408-7029078B-24B7-40D6-8E26-1570F72486D0 wds:Q66038408-8A5F41C0-FE77-483D-B54A-ED85C986DFE2 wds:Q66038408-9C1D81DD-BF9A-4E02-9186-ADD279DC84AE wds:Q66038408-BED9049A-CAD4-477C-B0EC-BC0AB2AA2687 wds:Q66038408-C0F2F93A-A923-422A-994A-EB6E11A5BB9B wds:Q66038408-C340CD8B-07AE-481A-98DB-D50A4B7D4855 wds:Q66038408-C6FE6444-EF12-428F-A015-9DC239A8DC45 wds:Q66038408-D3F40267-F01C-4C09-A9A4-56BB087C43E0
research site	Loyola University Medical Center University of Oklahoma Health Sciences Center Boston University University of Kansas Medical Center Swedish Medical Center Barbara Ann Karmanos Cancer Institute University of Cincinnati University of Tennessee, Knoxville Tulane University University of Mississippi Medical Center University of Michigan University of Utah Health Care Michigan Cancer Research Consortium Chao Family Comprehensive Cancer Center Harrington Cancer Center
minimum age	wds:Q66038408-3781C373-F2CD-4532-A455-E3FBE8870133
minimum age	18 (xsd:decimal)
number of participants	wds:Q66038408-0C6A9B30-E91B-42F6-AA74-23033B46DE18
number of participants	180 (xsd:decimal)
maximum age	wds:Q66038408-DE64AC18-C954-4E33-950B-CE713D807B4E
maximum age	120 (xsd:decimal)
study type	wds:Q66038408-AC05B48F-5A31-45DE-86F5-445C826AD852
study type	observational study
ClinicalTrials.gov ID	wds:Q66038408-5AD7E1DC-008F-4DDC-91D6-1F4A4DB1ED24
ClinicalTrials.gov ID	NCT00002900
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q66038408

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