ID

28154

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: Montral Cognitive Assessment (MoCA)

Stichworte

Versionen (3)
  1. 13.10.17 13.10.17 -
  2. 23.10.17 23.10.17 -
  3. 22.12.17 22.12.17 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

22. Dezember 2017

DOI

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

Englisch

MoCA GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulare  
MoCA General information
Beschreibung

MoCA General information

1. Date of visit/assessment
Beschreibung

Date of visit/assessment

Datentyp

date

Alias
UMLS CUI [1]
C1320303
Informed consent
Beschreibung

Informed consent

Datentyp

text

Alias
UMLS CUI [1]
C0021430
MoCA Eligibility Question
Beschreibung

MoCA Eligibility Question

1. Did subject meet all MoCA eligibility criteria?
Beschreibung

MoCA eligibility criteria met

Datentyp

text

Alias
UMLS CUI [1]
C1516637
[I51] 1. Availability of an approved translation
Beschreibung

Inclusion criterion

Datentyp

boolean

Alias
UMLS CUI [1]
C2348563
[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.
Beschreibung

Inclusion criterion

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
[E51] 1. Inability to complete all items on the MoCA due to physical limitation(s)
Beschreibung

Exclusion criterion

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0026606
UMLS CUI [1,2]
C0449295
Montreal Cognitive Assessment
Beschreibung

Montreal Cognitive Assessment

MoCA Status
Beschreibung

MoCA Status

Datentyp

text

Alias
UMLS CUI [1]
C3496286
Montreal Cognitive Assessment (MoCA)
Beschreibung

Montreal Cognitive Assessment (MoCA)

Datentyp

text

Alias
UMLS CUI [1]
C3496286
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Ähnliche Modelle

MoCA GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
MoCA General information
Date of visit/assessment
Item
1. Date of visit/assessment
date
C1320303 (UMLS CUI [1])
Informed consent
Item
Informed consent
text
C0021430 (UMLS CUI [1])
Item Group
MoCA Eligibility Question
Item
1. Did subject meet all MoCA eligibility criteria?
text
C1516637 (UMLS CUI [1])
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
C2348563 (UMLS CUI [1])
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
C0021430 (UMLS CUI [1])
physical limitation
Item
[E51] 1. Inability to complete all items on the MoCA due to physical limitation(s)
boolean
C0026606 (UMLS CUI [1,1])
C0449295 (UMLS CUI [1,2])
Item Group
Montreal Cognitive Assessment
MoCA Status
Item
MoCA Status
text
C3496286 (UMLS CUI [1])
Montreal Cognitive Assessment (MoCA)
Item
Montreal Cognitive Assessment (MoCA)
text
C3496286 (UMLS CUI [1])
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