ID

28262

Beskrivning

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)

Nyckelord

Versioner (4)
  1. 2017-09-27 2017-09-27 -
  2. 2017-10-04 2017-10-04 -
  3. 2017-10-23 2017-10-23 -
  4. 2018-01-01 2018-01-01 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

1 januari 2018

DOI

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Licens

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

Engelsk

Hospitalisation Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulär  
Hospitalisation
Beskrivning

Hospitalisation

1. Admission date
Beskrivning

Admission date

Datatyp

date

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

Discharge date

Datatyp

date

Alias
UMLS CUI [1]
C2361123
Discharge diagnoses
Beskrivning

Discharge diagnoses

3.a Sequence number
Beskrivning

[hidden]

Datatyp

text

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

Diagnosis at discharge

Datatyp

text

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

[hidden]

Datatyp

text

Alias
UMLS CUI [1]
C2826302
MedDRA synonym
Beskrivning

[hidden]

Datatyp

text

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

[hidden]

Datatyp

text

Alias
UMLS CUI [1]
C3898442
Failed coding
Beskrivning

[hidden]

Datatyp

text

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

Diagnosis type

Datatyp

integer

Alias
UMLS CUI [1]
C1550351
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Similar models

Hospitalisation Repeating form GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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)
Tillbaka till toppen 

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