0 Evaluaciones
ID

20421

Descripción

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

Palabras clave

Versiones (1)
  1. 22/2/17 22/2/17 -
Subido en

22 de febrero de 2017

DOI

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Licencia

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

    Inglés

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

    1 formularios  
    Trial Completion
    Descripción

    Trial Completion

    Alias
    UMLS CUI-1
    C2732579 (Completion of clinical trial)
    SNOMED
    443729008
    1. The patient completed planned observation time according to protocol
    Descripción

    patient completed planned observation time

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0525058 (Protocol Compliance)
    UMLS CUI [1,2]
    C0040223 (Time)
    SNOMED
    410670007
    LOINC
    LP73517-2
    2. If no please specify why:
    Descripción

    if no

    Tipo de datos

    integer

    Alias
    UMLS CUI [1]
    C2348235 (Specification)
    Explain:
    Descripción

    Explanation

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C0681841 (Explanation)
    LOINC
    LA15331-4
    Invenstigator´s Declaration
    Descripción

    Invenstigator´s Declaration

    Alias
    UMLS CUI-1
    C0008961 (Clinical Investigators)
    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.
    Descripción

    Invenstigator´s Declaration

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0008961 (Clinical Investigators)
    UMLS CUI [1,2]
    C1442085 (Instructions)
    LOINC
    LP6820-7
    Investigator´s signature
    Descripción

    Investigator´s signature

    Tipo de datos

    text

    Alias
    UMLS CUI [1]
    C2346576 (Investigator Signature)
    Date of Signature
    Descripción

    Date of Signature

    Tipo de datos

    date

    Alias
    UMLS CUI [1,1]
    C0011008 (Date in time)
    SNOMED
    410671006
    UMLS CUI [1,2]
    C1519316 (Signature)
    LOINC
    LP248948-4
    Volver a la parte superior de la página

    Similar models

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

    1 formularios
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    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])
    Volver a la parte superior de la página 

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