ID

28046

Description

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: Other Medical Conditions

Keywords

Versions (4)
  1. 8/27/17 8/27/17 -
  2. 10/13/17 10/13/17 -
  3. 10/23/17 10/23/17 -
  4. 12/12/17 12/12/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

December 12, 2017

DOI

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License

Creative Commons BY-NC 3.0
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Other Medical Conditions GSK study Chronic Coronary Heart Disease NCT00799903

English

Other Medical Conditions GSK study Chronic Coronary Heart Disease NCT00799903

1 forms  
Other medical conditions
Description

Other medical conditions

1. Is there a family history of premature CHD? (Male family member <55 years or female family member <65 years)
Description

family history cardiovascular risk factors

Data type

integer

Alias
UMLS CUI [1]
C0850624
2. Has subject had any history of cancer?
Description

history of cancer

Data type

integer

Alias
UMLS CUI [1]
C2735088
History of cancer
Description

History of cancer

1.a Specific condition
Description

Specific condition

Data type

integer

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348235
1.b Date of diagnosis
Description

Date of diagnosis

Data type

date

Alias
UMLS CUI [1]
C2316983
Sequence Number
Description

Sequence Number

Data type

text

Alias
UMLS CUI [1]
C2348184
Specific condition
Description

Specific condition

Data type

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348235
Modified Term
Description

Modified Term

Data type

text

Alias
UMLS CUI [1]
C2826302
MedDRA Synonym
Description

MedDRA Synonym

Data type

text

Alias
UMLS CUI [1]
C1140263
MedDRA lower level term code
Description

MedDRA lower level term code

Data type

text

Alias
UMLS CUI [1,1]
C2826302
UMLS CUI [1,2]
C1519255
Failed coding
Description

Failed coding

Data type

text

Alias
UMLS CUI [1,1]
C0805701
UMLS CUI [1,2]
C0231175
Date of diagnosis
Description

Date of diagnosis

Data type

date

Alias
UMLS CUI [1]
C2316983
Other history of cancer
Description

Other history of cancer

2.a Sequence Number
Description

Sequence Number other

Data type

text

Alias
UMLS CUI [1]
C2348184
2.b Specific Condition
Description

Specific Condition other

Data type

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348235
2.c Modified Term
Description

Modified Term other

Data type

text

Alias
UMLS CUI [1]
C2826302
MedDRA Synonym
Description

MedDRA Synonym other

Data type

text

Alias
UMLS CUI [1]
C1140263
MedDRA lower level term code
Description

MedDRA lower level term code other

Data type

text

Alias
UMLS CUI [1]
C3898442
Failed coding
Description

Failed coding other

Data type

text

Alias
UMLS CUI [1,1]
C0805701
UMLS CUI [1,2]
C0231175
2.d Date of diagnosis
Description

Date of diagnosis

Data type

date

Alias
UMLS CUI [1]
C2316983
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Similar models

Other Medical Conditions GSK study Chronic Coronary Heart Disease NCT00799903

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Other medical conditions
Item
1. Is there a family history of premature CHD? (Male family member <55 years or female family member <65 years)
integer
C0850624 (UMLS CUI [1])
family history of premature CHD
Code List
1. Is there a family history of premature CHD? (Male family member <55 years or female family member <65 years)
CL Item
Yes (1)
CL Item
No (0)
Item
2. Has subject had any history of cancer?
integer
C2735088 (UMLS CUI [1])
family history of premature CHD
Code List
2. Has subject had any history of cancer?
CL Item
Yes (1)
CL Item
No (0)
Item Group
History of cancer
Item
1.a Specific condition
integer
C0012634 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Specific condition
Code List
1.a Specific condition
CL Item
Benign neoplasm (1)
C0086692 (UMLS CUI-1)
(Comment:en)
CL Item
Bile duct cancer (2)
C0005400 (UMLS CUI-1)
(Comment:en)
CL Item
Bladder cancer (3)
C0005684 (UMLS CUI-1)
(Comment:en)
CL Item
Bowel cancer (4)
C0699790 (UMLS CUI-1)
(Comment:en)
CL Item
Breast cancer (5)
C0678222 (UMLS CUI-1)
(Comment:en)
CL Item
Cervical cancer (6)
C0007847 (UMLS CUI-1)
(Comment:en)
CL Item
Endometrial cancer (7)
C0476089 (UMLS CUI-1)
(Comment:en)
CL Item
Esophageal cancer (8)
C0014859 (UMLS CUI-1)
(Comment:en)
CL Item
Fallopian tube cancer (9)
C0015560 (UMLS CUI-1)
(Comment:en)
CL Item
Gallbladder cancer (10)
C0016976 (UMLS CUI-1)
(Comment:en)
CL Item
Gastric cancer (11)
CL Item
Hodgkin's disease (12)
CL Item
Leukemia (13)
CL Item
Lip cancer (14)
CL Item
Liver cancer (15)
CL Item
Lung cancer (16)
CL Item
Lymphoma (17)
CL Item
Multiple myeloma (18)
CL Item
Myelodysplastic syndrome (19)
CL Item
Non-melanoma skin cancer (20)
CL Item
Oral cancer (21)
CL Item
Ovarian cancer (22)
CL Item
Pancreatic cancer (23)
CL Item
Penile cancer (24)
CL Item
Pharyngeal cancer (25)
CL Item
Prostate cancer (26)
CL Item
Renal cancer (27)
CL Item
Scrotum cancer (28)
CL Item
Skin melanoma (29)
CL Item
Testicular cancer (30)
CL Item
Vaginal cancer (31)
CL Item
Vulval cancer (32)
Date of diagnosis
Item
1.b Date of diagnosis
date
C2316983 (UMLS CUI [1])
Sequence Number
Item
Sequence Number
text
C2348184 (UMLS CUI [1])
Specific condition
Item
Specific condition
text
C0012634 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Modified Term
Item
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
C2826302 (UMLS CUI [1,1])
C1519255 (UMLS CUI [1,2])
Failed coding
Item
Failed coding
text
C0805701 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
Date of diagnosis
Item
Date of diagnosis
date
C2316983 (UMLS CUI [1])
Item Group
Other history of cancer
Sequence Number other
Item
2.a Sequence Number
text
C2348184 (UMLS CUI [1])
Specific Condition other
Item
2.b Specific Condition
text
C0012634 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Modified Term other
Item
2.c Modified Term
text
C2826302 (UMLS CUI [1])
MedDRA Synonym other
Item
MedDRA Synonym
text
C1140263 (UMLS CUI [1])
MedDRA lower level term code other
Item
MedDRA lower level term code
text
C3898442 (UMLS CUI [1])
Failed coding other
Item
Failed coding
text
C0805701 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
Date of diagnosis
Item
2.d Date of diagnosis
date
C2316983 (UMLS CUI [1])
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