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ID

20421

Beschreibung

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

Stichworte

Versionen (1)
  1. 22.02.17 22.02.17 -
Hochgeladen am

22. Februar 2017

DOI

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Lizenz

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

    Englisch

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

    1 Formulare  
    Trial Completion
    Beschreibung

    Trial Completion

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

    patient completed planned observation time

    Datentyp

    boolean

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

    if no

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C2348235
    Explain:
    Beschreibung

    Explanation

    Datentyp

    text

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

    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.
    Beschreibung

    Invenstigator´s Declaration

    Datentyp

    text

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

    Investigator´s signature

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C2346576
    Date of Signature
    Beschreibung

    Date of Signature

    Datentyp

    date

    Alias
    UMLS CUI [1,1]
    C0011008
    UMLS CUI [1,2]
    C1519316
    Zum Seitenanfang zurückkehren

    Ähnliche Modelle

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

    1 Formulare
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    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])
    Zum Seitenanfang zurückkehren 

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