ID

20421

Beschrijving

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

Trefwoorden

Versies (1)
  1. 22-02-17 22-02-17 -
Geüploaded op

22 februari 2017

DOI

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Licentie

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

Engels

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

1 Formulieren  
Trial Completion
Beschrijving

Trial Completion

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

patient completed planned observation time

Datatype

boolean

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

if no

Datatype

integer

Alias
UMLS CUI [1]
C2348235
Explain:
Beschrijving

Explanation

Datatype

text

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

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.
Beschrijving

Invenstigator´s Declaration

Datatype

text

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

Investigator´s signature

Datatype

text

Alias
UMLS CUI [1]
C2346576
Date of Signature
Beschrijving

Date of Signature

Datatype

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1519316
Terug naar het begin van de pagina

Similar models

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

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

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