ID

20388

Descrição

The purpose of the trial is to determine if extended-release dipyridamole + aspirin [Aggrenox, Asasa ntin] is superior to clopidogrel [Plavix], and if telmisartan [Micardis, Gliosartan, Kinzal, Kinzalm ono, Predxal, Pritor, Samertan, Telmisartan] is superior to placebo, in the presence of background antihypertensive therapy, in prevention of a second stroke in patients who have recently suffered a stroke and therefore are at high risk of suffering another one. End of Trial Study Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00153062?term=NCT00153062&rank=1

Link

https://clinicaltrials.gov/ct2/show/NCT00153062?term=NCT00153062&rank=1

Palavras-chave

Versões (1)
  1. 21/02/2017 21/02/2017 -
Transferido a

21 de fevereiro de 2017

DOI

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Licença

Creative Commons BY 4.0
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End of Trial Concomitant Medication ACE Inhibitors PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

Inglês

End of Trial Concomitant Medication ACE Inhibitors PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

1 Formulários  
Concomitant Medication
Descrição

Concomitant Medication

Alias
UMLS CUI-1
C2347852
1. Since the visit 5, were any of the non-study medications listed below taken?
Descrição

Medication taken

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1553892
If yes, please indicate which of the following were being taken:
Descrição

If yes, please indicate which

Tipo de dados

integer

Alias
UMLS CUI [1]
C1553892
ACE Inhibitors
Descrição

ACE Inhibitors

Alias
UMLS CUI-1
C0003015
2. Since the visit 5, were any ACE inhibitors taken?
Descrição

ACE Inhibitors currently taken

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0013227
If Yes, please indicate which, and total daily dose:
Descrição

Name of ACE Inhibitor and Total Daily Dose

Tipo de dados

text

Alias
UMLS CUI [1,1]
C0003015
UMLS CUI [1,2]
C2360065
UMLS CUI [2,1]
C0003015
UMLS CUI [2,2]
C2348070
Restricted Concomitant Medication
Descrição

Restricted Concomitant Medication

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C0233470
3. Have any restricted medications in the categories defined on the opposite page been taken?
Descrição

Restricted medication taken

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1518384
UMLS CUI [1,2]
C0087111
If yes, please indicate which category
Descrição

if yes

Tipo de dados

integer

Alias
UMLS CUI [1]
C0683312
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Similar models

End of Trial Concomitant Medication ACE Inhibitors PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
Medication taken
Item
1. Since the visit 5, were any of the non-study medications listed below taken?
boolean
C1553892 (UMLS CUI [1])
Item
If yes, please indicate which of the following were being taken:
integer
C1553892 (UMLS CUI [1])
If yes, please indicate which
Code List
If yes, please indicate which of the following were being taken:
CL Item
Parental anticoagulants (Short term use) (1)
CL Item
Oral anticoagulants (Short term use) (2)
CL Item
Nitrates (oral or topical) (3)
CL Item
Estrogen replacement without progesterone (4)
CL Item
Estrogen replacement with progesterone (5)
CL Item
Digitalis (6)
CL Item
Statins (7)
CL Item
Fibrates (8)
CL Item
Dilitazem/Verapamil (9)
CL Item
Other calcium channel blockers (10)
CL Item
Alpha-blocker (11)
CL Item
Direct vasodilators (12)
CL Item
Peripheral sympatholytic (13)
CL Item
Central sympatholytic (14)
CL Item
Alpha-beta blocker (15)
CL Item
Beta-blocker (16)
CL Item
Loop-active diuretics (17)
CL Item
Diuretics of thiazide type (18)
CL Item
Potassium-sparing diuretics (19)
CL Item
Insulin (20)
CL Item
Oral hypoglycemic agents (21)
CL Item
Specific Cox II inhibitors (22)
Item Group
ACE Inhibitors
C0003015 (UMLS CUI-1)
ACE Inhibitors currently taken
Item
2. Since the visit 5, were any ACE inhibitors taken?
boolean
C0013227 (UMLS CUI [1])
Name of ACE Inhibitor and Total Daily Dose
Item
If Yes, please indicate which, and total daily dose:
text
C0003015 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
C0003015 (UMLS CUI [2,1])
C2348070 (UMLS CUI [2,2])
Item Group
Restricted Concomitant Medication
C2347852 (UMLS CUI-1)
C0233470 (UMLS CUI-2)
Restricted medication taken
Item
3. Have any restricted medications in the categories defined on the opposite page been taken?
boolean
C1518384 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Item
If yes, please indicate which category
integer
C0683312 (UMLS CUI [1])
if yes
Code List
If yes, please indicate which category
CL Item
1 (1)
CL Item
2 (2)
CL Item
3 (3)
CL Item
4 (4)
CL Item
5 (5)
CL Item
6 (6)
CL Item
7 (7)
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