ID

25733

Beschreibung

Study ID: 100601 Clinical Study ID: LPL100601 Study Title: LPL100601, A Clinical Outcomes Study of Darapladib versus Placebo in Subjects with Chronic Coronary Heart Disease to Compare the Incidence of Major Adverse Cardiovascular Events (MACE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00799903 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: darapladib Study Indication: Atherosclerosis Study part: Cognitive Function Substudy.

Stichworte

Versionen (5)
  1. 15.09.17 15.09.17 -
  2. 21.09.17 21.09.17 -
  3. 13.10.17 13.10.17 -
  4. 23.10.17 23.10.17 -
  5. 20.12.17 20.12.17 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

15. September 2017

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.

Cognitive Function Substudy GSK study Chronic Coronary Heart Disease NCT00799903

Englisch

Cognitive Function Substudy GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulare  
Cognitive Function Eligibility Question
Beschreibung

Cognitive Function Eligibility Question

1. Did the subject meet all the Cognitive Function substudy entry criteria?
Beschreibung

No, please select all boxes corresponding to violations of any inclusion/exclusion criteria

Datentyp

text

[I08] Cognitive Function 1. Signed written informed consent prior to beginning substudy-related procedures (subject must understand the aims, investigational procedures and possible consequences of the substudy).
Beschreibung

Inclusion criterion. Note: Consent to participate in the substudy is separate from consent to participate in the parent study.

Datentyp

boolean

[I09] Cognitive Function 2. Adequate vision and hearing for neuropsychological testing.
Beschreibung

Inclusion criterion.

Datentyp

boolean

[E22] Cognitive Function 1. High level of cognitive function as assessed by a score of >50 on the Symbol Digit Modalities Test.
Beschreibung

Exclusion criterion.

Datentyp

boolean

[E23] Cognitive Function 2. Significant deficit in verbal intelligence as assessed by Adult Reading Test score <85.
Beschreibung

Exclusion criterion.

Datentyp

boolean

[E24] Cognitive Function 3. Aphasia
Beschreibung

Exclusion criterion.

Datentyp

boolean

[E25] Cognitive Function 4. Inability to perform the test due to significant weakness in dominant hand.
Beschreibung

Exclusion criterion.

Datentyp

boolean

Cognitive Function substudy
Beschreibung

Cognitive Function substudy

1. Cognitive function testing completed
Beschreibung

cognitive function testing completed

Datentyp

text

1. Date cognitive function testing completed
Beschreibung

Date cognitive function testing

Datentyp

date

Zum Seitenanfang zurückkehren

Ähnliche Modelle

Cognitive Function Substudy GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Cognitive Function Eligibility Question
Item
1. Did the subject meet all the Cognitive Function substudy entry criteria?
text
Cognitive Function substudy entry criteria met
Code List
1. Did the subject meet all the Cognitive Function substudy entry criteria?
CL Item
Yes (Y)
CL Item
No, please select all boxes corresponding to violations of any inclusion/exclusion criteria (N)
Informed consent
Item
[I08] Cognitive Function 1. Signed written informed consent prior to beginning substudy-related procedures (subject must understand the aims, investigational procedures and possible consequences of the substudy).
boolean
Vision and hearing
Item
[I09] Cognitive Function 2. Adequate vision and hearing for neuropsychological testing.
boolean
High level cognitive function
Item
[E22] Cognitive Function 1. High level of cognitive function as assessed by a score of >50 on the Symbol Digit Modalities Test.
boolean
deficit in verbal intelligence
Item
[E23] Cognitive Function 2. Significant deficit in verbal intelligence as assessed by Adult Reading Test score <85.
boolean
Aphasia
Item
[E24] Cognitive Function 3. Aphasia
boolean
weakness in dominant hand
Item
[E25] Cognitive Function 4. Inability to perform the test due to significant weakness in dominant hand.
boolean
Item Group
Cognitive Function substudy
Item
1. Cognitive function testing completed
text
cognitive function testing completed
Code List
1. Cognitive function testing completed
CL Item
Date (-99)
CL Item
Not done (ND)
Date cognitive function testing
Item
1. Date cognitive function testing completed
date
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