ID

29525

Beschreibung

Study ID: 102871 Clinical Study ID: HZC102871 Study Title:HZC102871: A 52-week efficacy and safety study to compare the effect of three dosage strengths of Fluticasone Furoate/GW642444 Inhalation Powder with GW642444 on the Annual Rate of Exacerbations in Subjects with Chronic Obstructive Pulmonary Disease (COPD) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01009463 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate Trade Name: Veramyst,Avamys,Allermist Study Indication: Pulmonary Disease, Chronic Obstructive Documentation part: LOG Status

Stichworte

Versionen (2)
  1. 04.03.18 04.03.18 -
  2. 05.04.18 05.04.18 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

5. April 2018

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY-NC 3.0
Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Zurück zu Modell Kommentaren
Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

GSK Efficacy and safety of Fluticasone on the Annual Rate of Exacerbations in Subjects with Chronic Obstructive Pulmonary Disease (COPD) NCT01009463

Englisch

LOG Status

1 Formulare  
  1. StudyEvent: ODM
    1. LOG Status
LOG Status
Beschreibung

LOG Status

Alias
UMLS CUI-1
C1708728
UMLS CUI-2
C0449438
Were any concomitant medications taken by the subject during the study?
Beschreibung

Concomitant medications

Datentyp

boolean

Alias
UMLS CUI [1]
C2347852
Did the subject experience any non-serious adverse events during the study?
Beschreibung

non-serious adverse event

Datentyp

boolean

Alias
UMLS CUI [1]
C1518404
Did the subject experience any COPD exacerbations?
Beschreibung

COPD exacerbations

Datentyp

boolean

Alias
UMLS CUI [1]
C0740304
Has subject been diagnosed with pneumonia?
Beschreibung

pneumonia

Datentyp

boolean

Alias
UMLS CUI [1]
C0032285
Did the subject have a fracture during the course of the study?
Beschreibung

fracture

Datentyp

boolean

Alias
UMLS CUI [1]
C0016658
Did any Novel Dry Powder Inhaler device(s) supplied to the subject malfunction during the course of the study?
Beschreibung

device malfunction

Datentyp

boolean

Alias
UMLS CUI [1]
C0025080
Zum Seitenanfang zurückkehren

Ähnliche Modelle

LOG Status

1 Formulare
  1. StudyEvent: ODM
    1. LOG Status
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
LOG Status
C1708728 (UMLS CUI-1)
C0449438 (UMLS CUI-2)
Concomitant medications
Item
Were any concomitant medications taken by the subject during the study?
boolean
C2347852 (UMLS CUI [1])
non-serious adverse event
Item
Did the subject experience any non-serious adverse events during the study?
boolean
C1518404 (UMLS CUI [1])
COPD exacerbations
Item
Did the subject experience any COPD exacerbations?
boolean
C0740304 (UMLS CUI [1])
pneumonia
Item
Has subject been diagnosed with pneumonia?
boolean
C0032285 (UMLS CUI [1])
fracture
Item
Did the subject have a fracture during the course of the study?
boolean
C0016658 (UMLS CUI [1])
device malfunction
Item
Did any Novel Dry Powder Inhaler device(s) supplied to the subject malfunction during the course of the study?
boolean
C0025080 (UMLS CUI [1])
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video