ID

20421

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. 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. 22/02/2017 22/02/2017 -
Transferido a

22 de fevereiro de 2017

DOI

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Licença

Creative Commons BY 4.0
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Trial Completion PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

Inglês

Trial Completion PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

1 Formulários  
Trial Completion
Descrição

Trial Completion

Alias
UMLS CUI-1
C2732579
1. The patient completed planned observation time according to protocol
Descrição

patient completed planned observation time

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0040223
2. If no please specify why:
Descrição

if no

Tipo de dados

integer

Alias
UMLS CUI [1]
C2348235
Explain:
Descrição

Explanation

Tipo de dados

text

Alias
UMLS CUI [1]
C0681841
Invenstigator´s Declaration
Descrição

Invenstigator´s Declaration

Alias
UMLS CUI-1
C0008961
3. Invenstigator´s Declaration By signing and dating this page, I declare that I have reviewed for accuracy all case report form pages for this patient; the information contained on these pages accurately reflects the medical record including the results of tests and evaluations performed in the dates specified.
Descrição

Invenstigator´s Declaration

Tipo de dados

text

Alias
UMLS CUI [1,1]
C0008961
UMLS CUI [1,2]
C1442085
Investigator´s signature
Descrição

Investigator´s signature

Tipo de dados

text

Alias
UMLS CUI [1]
C2346576
Date of Signature
Descrição

Date of Signature

Tipo de dados

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1519316
Voltar ao início da página

Similar models

Trial Completion PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Trial Completion
C2732579 (UMLS CUI-1)
patient completed planned observation time
Item
1. The patient completed planned observation time according to protocol
boolean
C0525058 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Item
2. If no please specify why:
integer
C2348235 (UMLS CUI [1])
if no
Code List
2. If no please specify why:
CL Item
Death (must me recorded on death form) (1)
CL Item
Adverse Event (explain below) (2)
CL Item
Non compliant with protocol (explain below) (3)
CL Item
Lost follow-up (explain below) (4)
CL Item
Consent withdrawn (not due to adverse event, explain below) (5)
CL Item
Other (explain below) (6)
Explanation
Item
Explain:
text
C0681841 (UMLS CUI [1])
Item Group
Invenstigator´s Declaration
C0008961 (UMLS CUI-1)
Invenstigator´s Declaration
Item
3. Invenstigator´s Declaration By signing and dating this page, I declare that I have reviewed for accuracy all case report form pages for this patient; the information contained on these pages accurately reflects the medical record including the results of tests and evaluations performed in the dates specified.
text
C0008961 (UMLS CUI [1,1])
C1442085 (UMLS CUI [1,2])
Investigator´s signature
Item
Investigator´s signature
text
C2346576 (UMLS CUI [1])
Date of Signature
Item
Date of Signature
date
C0011008 (UMLS CUI [1,1])
C1519316 (UMLS CUI [1,2])
Voltar ao início da página 

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