ID

28313

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: Cardiovascular diagnostic procedures

Trefwoorden

Versies (4)
  1. 05-10-17 05-10-17 -
  2. 05-10-17 05-10-17 -
  3. 23-10-17 23-10-17 -
  4. 03-01-18 03-01-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

3 januari 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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Cardiovascular diagnostic procedures GSK study Chronic Coronary Heart Disease NCT00799903

Engels

Cardiovascular diagnostic procedures GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren  
Cardiovascular diagnostic procedures
Beschrijving

Cardiovascular diagnostic procedures

1.a Specific procedure
Beschrijving

Specific cardiovascular diagnostic procedure

Datatype

integer

Alias
UMLS CUI [1]
C0189573
1.b Date of Procedure
Beschrijving

Date and time are optional.

Datatype

date

Alias
UMLS CUI [1,1]
C0430022
UMLS CUI [1,2]
C0011008
Cardiac stress testing
Beschrijving

Cardiac stress testing

2.a Specific procedure
Beschrijving

Cardiac stress testing specific procedure

Datatype

integer

Alias
UMLS CUI [1]
C3272313
2.b Date of Procedure
Beschrijving

Date and time are optional.

Datatype

date

Alias
UMLS CUI [1,1]
C3272313
UMLS CUI [1,2]
C0011008
Other cardiac diagnostic procedures
Beschrijving

Other cardiac diagnostic procedures

3.a Sequence Number
Beschrijving

[hidden] Item is not required

Datatype

text

Alias
UMLS CUI [1]
C2348184
3.b Specific Procedure
Beschrijving

Date and time are optional.

Datatype

text

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C1521902
3.c Modified Term
Beschrijving

[hidden] Item is not required

Datatype

text

Alias
UMLS CUI [1]
C2826302
MedDRA Synonym
Beschrijving

[hidden]

Datatype

text

Alias
UMLS CUI [1]
C1140263
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 Date of Procedure
Beschrijving

Date of Other Procedure

Datatype

date

Alias
UMLS CUI [1]
C2584899
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Similar models

Cardiovascular diagnostic procedures GSK study Chronic Coronary Heart Disease NCT00799903

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Cardiovascular diagnostic procedures
Item
1.a Specific procedure
integer
C0189573 (UMLS CUI [1])
Specific procedure
Code List
1.a Specific procedure
CL Item
Cardiac catheterization (1)
C0018795 (UMLS CUI-1)
(Comment:en)
CL Item
Cardiac MRI (2)
C0024485 (UMLS CUI-1)
(Comment:en)
CL Item
Cardiac CT (3)
C0412618 (UMLS CUI-1)
(Comment:en)
CL Item
Echocardiogram (4)
C0013516 (UMLS CUI-1)
(Comment:en)
Date of cardiovascular diagnostic procedure
Item
1.b Date of Procedure
date
C0430022 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Cardiac stress testing
Item
2.a Specific procedure
integer
C3272313 (UMLS CUI [1])
Specific procedure
Code List
2.a Specific procedure
CL Item
Exercise echocardiogram (5)
C2035955 (UMLS CUI-1)
(Comment:en)
CL Item
Exercise test with imaging (6)
C0015260 (UMLS CUI-1)
(Comment:en)
CL Item
Stress echocardiogram (7)
C0920208 (UMLS CUI-1)
(Comment:en)
CL Item
Pharmacological stress echocardiogram (8)
C0920208 (UMLS CUI-1)
(Comment:en)
CL Item
Pharmacological stress test with imaging (9)
C0920208 (UMLS CUI-1)
C0011923 (UMLS CUI-2)
(Comment:en)
CL Item
Exercise echocardiogram test without imaging (10)
C2035955 (UMLS CUI-1)
(Comment:en)
2.b Date of cardiac stress testing
Item
2.b Date of Procedure
date
C3272313 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Other cardiac diagnostic procedures
Sequence Number
Item
3.a Sequence Number
text
C2348184 (UMLS CUI [1])
Specific Other Procedure
Item
3.b Specific Procedure
text
C0184661 (UMLS CUI [1,1])
C1521902 (UMLS CUI [1,2])
Modified Term
Item
3.c Modified Term
text
C2826302 (UMLS CUI [1])
MedDRA Synonym
Item
MedDRA Synonym
text
C1140263 (UMLS CUI [1])
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])
Date of Other Procedure
Item
3.d Date of Procedure
date
C2584899 (UMLS CUI [1])
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