About: Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding

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About: Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding 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)
rdfs:label	Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding (en)
skos:prefLabel	Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding (en)
name	Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding (en)
title	wds:Q64808506-D223E389-711A-4543-A85B-ACBFB145A277
title	Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding Endometrial Volume as a Predictor of Endometrial Pathology in Perimenopausal Uterine Bleeding (en)
end time	wds:Q64808506-51E2A715-3B65-4CED-88A0-F8CAE4E2F8E3
end time	2018-08-01 00:00:00Z (xsd:dateTime)
instance of	wds:Q64808506-250BC9D2-1A81-4E61-8474-1154395EE98F
instance of	clinical trial
start time	wds:Q64808506-B6E33CA9-ADDE-4FF0-95A4-F7CD249E2FAB
start time	2017-08-08 00:00:00Z (xsd:dateTime)
country	wds:Q64808506-B42FC371-C31B-4730-BF13-7AF7932BEAE2
country	Egypt
research site	wds:Q64808506-FC725F12-48BE-41B3-B535-E7A24F609AAD
research site	Mansoura University Hospital
minimum age	wds:Q64808506-6BC2283C-4DC9-4696-8ECA-4681BEAC0B04
minimum age	45 (xsd:decimal)
number of participants	wds:Q64808506-691821D9-F568-43AF-96DF-0B2DA802C798
number of participants	100 (xsd:decimal)
maximum age	wds:Q64808506-FFA14070-9755-4FCB-ABE6-5740F9BEE554
maximum age	55 (xsd:decimal)
study type	wds:Q64808506-8352F266-FB2B-4259-8EE8-D2121C1429F6
study type	interventional study
ClinicalTrials.gov ID	wds:Q64808506-E45A20F0-EE1A-4B78-BE35-4D3CC919153F
ClinicalTrials.gov ID	NCT03351673
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q64808506

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