ID

28262

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: Hospitalisation - Repeating form (Scheduled visits)

Trefwoorden

Versies (4)
  1. 27-09-17 27-09-17 -
  2. 04-10-17 04-10-17 -
  3. 23-10-17 23-10-17 -
  4. 01-01-18 01-01-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

1 januari 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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Hospitalisation Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

Engels

Hospitalisation Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren  
Hospitalisation
Beschrijving

Hospitalisation

1. Admission date
Beschrijving

Admission date

Datatype

date

Alias
UMLS CUI [1]
C1302393
2. Discharge date
Beschrijving

Discharge date

Datatype

date

Alias
UMLS CUI [1]
C2361123
Discharge diagnoses
Beschrijving

Discharge diagnoses

3.a Sequence number
Beschrijving

[hidden]

Datatype

text

Alias
UMLS CUI [1]
C2348184
3.b Diagnosis at discharge
Beschrijving

Diagnosis at discharge

Datatype

text

Alias
UMLS CUI [1]
C1555319
3.c Modified term
Beschrijving

[hidden]

Datatype

text

Alias
UMLS CUI [1]
C2826302
MedDRA synonym
Beschrijving

[hidden]

Datatype

text

Alias
UMLS CUI [1,1]
C0871468
UMLS CUI [1,2]
C1518404
MedDRA lower level term code
Beschrijving

[hidden]

Datatype

text

Alias
UMLS CUI [1]
C3898442
Failed coding
Beschrijving

[hidden]

Datatype

text

Alias
UMLS CUI [1,1]
C0805701
UMLS CUI [1,2]
C0231175
3.d Diagnosis type
Beschrijving

Diagnosis type

Datatype

integer

Alias
UMLS CUI [1]
C1550351
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Similar models

Hospitalisation Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Hospitalisation
Admission date
Item
1. Admission date
date
C1302393 (UMLS CUI [1])
Discharge date
Item
2. Discharge date
date
C2361123 (UMLS CUI [1])
Item Group
Discharge diagnoses
Sequence number
Item
3.a Sequence number
text
C2348184 (UMLS CUI [1])
Diagnosis at discharge
Item
3.b Diagnosis at discharge
text
C1555319 (UMLS CUI [1])
Modified term
Item
3.c Modified term
text
C2826302 (UMLS CUI [1])
MedDRA synonym
Item
MedDRA synonym
text
C0871468 (UMLS CUI [1,1])
C1518404 (UMLS CUI [1,2])
MedDRA lower level term code
Item
MedDRA lower level term code
text
C3898442 (UMLS CUI [1])
Failed coding
Item
Failed coding
text
C0805701 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
Item
3.d Diagnosis type
integer
C1550351 (UMLS CUI [1])
Diagnosis type
Code List
3.d Diagnosis type
CL Item
Primary diagnosis (1)
C0332137 (UMLS CUI-1)
(Comment:en)
CL Item
Secondary diagnosis (2)
C0332138 (UMLS CUI-1)
(Comment:en)
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