ID

25854

Beschrijving

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: Montral Cognitive Assessment (MoCA)

Trefwoorden

Versies (1)
  1. 21-09-17 21-09-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

21 september 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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MoCA GSK study Chronic Coronary Heart Disease NCT00799903

Engels

MoCA GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren  
MoCA General information
Beschrijving

MoCA General information

1. Date of visit/assessment
Beschrijving

Date of visit/assessment

Datatype

date

Informed consent
Beschrijving

Informed consent

Datatype

text

MoCA Eligibility Question
Beschrijving

MoCA Eligibility Question

1. Did subject meet all MoCA eligibility criteria?
Beschrijving

MoCA eligibility criteria met

Datatype

text

[I51] 1. Availability of an approved translation
Beschrijving

Inclusion criterion

Datatype

boolean

[I52] 2. Signed written informed consent prior to assessing the MoCA. Note: Consent to participate in the MoCA assessment is seperate from consent to participate in the parent study.
Beschrijving

Inclusion criterion

Datatype

boolean

[E51] 1. Inability to complete all items on the MoCA due to physical limitation(s)
Beschrijving

Exclusion criterion

Datatype

boolean

Montreal Cognitive Assessment
Beschrijving

Montreal Cognitive Assessment

MoCA Status
Beschrijving

MoCA Status

Datatype

text

Montreal Cognitive Assessment (MoCA)
Beschrijving

Montreal Cognitive Assessment (MoCA)

Datatype

text

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Similar models

MoCA GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
MoCA General information
Date of visit/assessment
Item
1. Date of visit/assessment
date
Informed consent
Item
Informed consent
text
Item Group
MoCA Eligibility Question
Item
1. Did subject meet all MoCA eligibility criteria?
text
MoCA eligibility criteria met
Code List
1. Did subject meet all MoCA eligibility criteria?
CL Item
Yes (Y)
CL Item
No, please select all boxes corresponding to the criteria that were not met (N)
Availability of an approved translation
Item
[I51] 1. Availability of an approved translation
boolean
informed consent
Item
[I52] 2. Signed written informed consent prior to assessing the MoCA. Note: Consent to participate in the MoCA assessment is seperate from consent to participate in the parent study.
boolean
physical limitation
Item
[E51] 1. Inability to complete all items on the MoCA due to physical limitation(s)
boolean
Item Group
Montreal Cognitive Assessment
MoCA Status
Item
MoCA Status
text
Montreal Cognitive Assessment (MoCA)
Item
Montreal Cognitive Assessment (MoCA)
text
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