ID

28052

Descripción

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: ABPM Substudy.

Palabras clave

Versiones (4)
  1. 15/9/17 15/9/17 -
  2. 13/10/17 13/10/17 -
  3. 23/10/17 23/10/17 -
  4. 12/12/17 12/12/17 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

12 de diciembre de 2017

DOI

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Licencia

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

Inglés

ABPM Substudy GSK study Chronic Coronary Heart Disease NCT00799903

1 formularios  
ABPM Substudy Participation
Descripción

ABPM Substudy Participation

1. Is the subject participating in the ABPM substudy?
Descripción

ABPM substudy participation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
No, select the reason why the subject is not participating in the ABPM substudy
Descripción

In case of "Inclusion [I] / exclusion [E] criteria", choose any criteria that apply in the following. In case of "Other", please specify in the following.

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0558080
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C0392360
[I06] ABPM 1. Signed written informed consent prior to beginning substudy-related procedures (subject must understand the aims, investigational procedures and possible consequences of the substudy).
Descripción

Note: Consent to participate in the substudy is separate from consent to participate in the parent study.

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
[I07] ABPM 2. Subjects must meet the following BP criteria one day before the parent study Baseline Visit. Subjects without diabetes mellitus or chronic kidney disease: BP <140/90mmHg. Subjects with diabetes mellitus or chronic kidney disease: BP <130/80mmHg.
Descripción

Chronic kidney disease is defined by either: reduced excretory function with an eGFR <60 mL/min per 1.73m2 (corresponding approximately to a creatinine of >1.5 mg/dL [132.6 S?mol/L] in men or >1.3 mg/dL [114.9 S?mol/L] in women) OR the presence of albuminuria (>300 mg/day or 200 mg albumin per gram of creatinine).

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C0243161
[E17] ABPM 1. Any changes in antihypertensive medications within the past 6 weeks.
Descripción

changes in antihypertensive medications

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003364
[E18] ABPM 2. Current atrial fibrillation.
Descripción

Current atrial fibrillation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004238
[E19] ABPM 3. Subjects who are expected to require a change in antihypertensive medication prior to the Month 3 visit.
Descripción

expected change in antihypertensive medication

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003364
[E20] ABPM 4. Subjects with an upper arm diameter of >42 cm.
Descripción

upper arm diameter of >42 cm

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0446516
UMLS CUI [1,2]
C0332520
[E21] ABPM 5. Subjects who work at night or whose work schedule includes rotating night time (10:00 PM to 6:00 AM) work.
Descripción

night time work

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1658633
UMLS CUI [1,2]
C1659095
[OT] Other, specify
Descripción

Other specification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C2348235
Medical condition - ABPM substudy
Descripción

Medical condition - ABPM substudy

1. Chronic kidney disease
Descripción

>300 mg/day or 200 mg albumin per gram of creatinine OR eGFR <60 mL//min per 1.73m2

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C2074731
ABPM substudy
Descripción

ABPM substudy

1. Was the ABPM device placed on the subject?
Descripción

ABPM device placed on subject

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0026426
UMLS CUI [1,2]
C0439841
Yes, date
Descripción

Date of placement of ABPM device

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0021107
UMLS CUI [1,3]
C0026426
No, provide reason
Descripción

No placement of ABPM device reason

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0026426
UMLS CUI [1,2]
C0025080
2. Was the ABPM data capture successful?
Descripción

ABPM data capture success

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3258067
UMLS CUI [1,2]
C0025080
If not succesful, did the subject wear the ABPM for 24 hours?
Descripción

ABPM for 24 hours

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0026426
If not succesful, will the ABPM be repeated?
Descripción

repetition of ABPM

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0589243
UMLS CUI [1,2]
C0026426
If no repetition, provide reason
Descripción

no repetition of ABPM reason

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0026426
UMLS CUI [1,2]
C0205341
ABPM substudy - Repeat assessments
Descripción

ABPM substudy - Repeat assessments

1. Was the ABPM device placed on the subject?
Descripción

ABPM device placed on subject repeat

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0026426
Yes, date
Descripción

Date of placement of ABPM device repeat

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0026426
UMLS CUI [1,3]
C0025080
UMLS CUI [1,4]
C0021107
No, provide reason
Descripción

No placement of ABPM device reason repeat

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0025080
UMLS CUI [1,2]
C0026426
2. Was the ABPM data capture successful?
Descripción

ABPM data capture success repeat

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0026426
If not succesful, did the subject wear the ABPM for 24 hours?
Descripción

ABPM for 24 hours repeat

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0026426
If not succesful, will the ABPM be repeated?
Descripción

repetition of ABPM repeat

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0026426
If no repetition, provide reason
Descripción

no repetition of ABPM reason repeat

Tipo de datos

text

Alias
UMLS CUI [1]
C0026426
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Similar models

ABPM Substudy GSK study Chronic Coronary Heart Disease NCT00799903

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
ABPM Substudy Participation
ABPM substudy participation
Item
1. Is the subject participating in the ABPM substudy?
boolean
C2348568 (UMLS CUI [1])
Item
No, select the reason why the subject is not participating in the ABPM substudy
text
C0558080 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
no participation reason
Code List
No, select the reason why the subject is not participating in the ABPM substudy
CL Item
Inclusion [I] / exclusion [E] criteria ([1])
CL Item
Site nor participating ([2])
CL Item
Other ([OT])
Informed consent
Item
[I06] ABPM 1. Signed written informed consent prior to beginning substudy-related procedures (subject must understand the aims, investigational procedures and possible consequences of the substudy).
boolean
C0021430 (UMLS CUI [1])
BP criteria
Item
[I07] ABPM 2. Subjects must meet the following BP criteria one day before the parent study Baseline Visit. Subjects without diabetes mellitus or chronic kidney disease: BP <140/90mmHg. Subjects with diabetes mellitus or chronic kidney disease: BP <130/80mmHg.
boolean
C0005823 (UMLS CUI [1,1])
C0243161 (UMLS CUI [1,2])
changes in antihypertensive medications
Item
[E17] ABPM 1. Any changes in antihypertensive medications within the past 6 weeks.
boolean
C0003364 (UMLS CUI [1])
Current atrial fibrillation
Item
[E18] ABPM 2. Current atrial fibrillation.
boolean
C0004238 (UMLS CUI [1])
expected change in antihypertensive medication
Item
[E19] ABPM 3. Subjects who are expected to require a change in antihypertensive medication prior to the Month 3 visit.
boolean
C0003364 (UMLS CUI [1])
upper arm diameter of >42 cm
Item
[E20] ABPM 4. Subjects with an upper arm diameter of >42 cm.
boolean
C0446516 (UMLS CUI [1,1])
C0332520 (UMLS CUI [1,2])
night time work
Item
[E21] ABPM 5. Subjects who work at night or whose work schedule includes rotating night time (10:00 PM to 6:00 AM) work.
boolean
C1658633 (UMLS CUI [1,1])
C1659095 (UMLS CUI [1,2])
Other specification
Item
[OT] Other, specify
text
C0205394 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Item Group
Medical condition - ABPM substudy
Item
1. Chronic kidney disease
integer
C1561643 (UMLS CUI [1,1])
C2074731 (UMLS CUI [1,2])
Chronic kidney disease
Code List
1. Chronic kidney disease
CL Item
Current (1)
CL Item
No medical condition (5)
Item Group
ABPM substudy
ABPM device placed on subject
Item
1. Was the ABPM device placed on the subject?
boolean
C0026426 (UMLS CUI [1,1])
C0439841 (UMLS CUI [1,2])
Date of placement of ABPM device
Item
Yes, date
date
C0011008 (UMLS CUI [1,1])
C0021107 (UMLS CUI [1,2])
C0026426 (UMLS CUI [1,3])
No placement of ABPM device reason
Item
No, provide reason
text
C0026426 (UMLS CUI [1,1])
C0025080 (UMLS CUI [1,2])
ABPM data capture success
Item
2. Was the ABPM data capture successful?
boolean
C3258067 (UMLS CUI [1,1])
C0025080 (UMLS CUI [1,2])
ABPM for 24 hours
Item
If not succesful, did the subject wear the ABPM for 24 hours?
boolean
C0026426 (UMLS CUI [1])
repetition of ABPM
Item
If not succesful, will the ABPM be repeated?
boolean
C0589243 (UMLS CUI [1,1])
C0026426 (UMLS CUI [1,2])
no repetition of ABPM reason
Item
If no repetition, provide reason
text
C0026426 (UMLS CUI [1,1])
C0205341 (UMLS CUI [1,2])
Item Group
ABPM substudy - Repeat assessments
ABPM device placed on subject repeat
Item
1. Was the ABPM device placed on the subject?
boolean
C0026426 (UMLS CUI [1])
Date of placement of ABPM device repeat
Item
Yes, date
date
C0011008 (UMLS CUI [1,1])
C0026426 (UMLS CUI [1,2])
C0025080 (UMLS CUI [1,3])
C0021107 (UMLS CUI [1,4])
No placement of ABPM device reason repeat
Item
No, provide reason
text
C0025080 (UMLS CUI [1,1])
C0026426 (UMLS CUI [1,2])
ABPM data capture success repeat
Item
2. Was the ABPM data capture successful?
boolean
C0026426 (UMLS CUI [1])
ABPM for 24 hours repeat
Item
If not succesful, did the subject wear the ABPM for 24 hours?
boolean
C0026426 (UMLS CUI [1])
repetition of ABPM repeat
Item
If not succesful, will the ABPM be repeated?
boolean
C0026426 (UMLS CUI [1])
no repetition of ABPM reason repeat
Item
If no repetition, provide reason
text
C0026426 (UMLS CUI [1])
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