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ID

20308

Description

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. Visit 1 (Month 0) Study Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00153062?term=NCT00153062&rank=1

Lien

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

Mots-clés

Versions (2)
  1. 15/02/2017 15/02/2017 -
  2. 20/02/2017 20/02/2017 -
Téléchargé le

20 février 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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    Visit 1 Month 0 Toast Criteria Concomitant Medication ACE Inhibitors PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

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    Visit 1 Month 0 Toast Criteria Concomitant Medication ACE Inhibitors PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

    1 Formulaires  
    Toast Criteria
    Description

    Toast Criteria

    Alias
    UMLS CUI-1
    C1710306
    For the qualifying stroke, please categories the etiologic subtype below (indicate one only)
    Description

    Etiologic subtype

    Type de données

    integer

    Alias
    UMLS CUI [1,1]
    C0038454
    UMLS CUI [1,2]
    C0015127
    Concomitant Medication
    Description

    Concomitant Medication

    Alias
    UMLS CUI-1
    C2347852
    Are any medications listed below currently being taken on the day of visit 1?
    Description

    Medication taken

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1553892
    If yes, please indicate which, if any, of the following are currently being taken:
    Description

    If the patient is taking any restricted (bolded) concomitant medications (see facing page), please ensure these are stopped prior to randomasation.

    Type de données

    integer

    Alias
    UMLS CUI [1]
    C1553892
    ACE Inhibitors
    Description

    ACE Inhibitors

    Alias
    UMLS CUI-1
    C0003015
    Are ACE Inhibitors currently being taken on the day of visit 1?
    Description

    ACE Inhibitors currently taken

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0013227
    Name of ACE Inhibitor and Total Daily Dose
    Description

    Name of ACE Inhibitor and Total Daily Dose

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0003015
    UMLS CUI [1,2]
    C2360065
    UMLS CUI [2,1]
    C0003015
    UMLS CUI [2,2]
    C2348070
    Retour au début de la page

    Similar models

    Visit 1 Month 0 Toast Criteria Concomitant Medication ACE Inhibitors PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Toast Criteria
    C1710306 (UMLS CUI-1)
    Item
    For the qualifying stroke, please categories the etiologic subtype below (indicate one only)
    integer
    C0038454 (UMLS CUI [1,1])
    C0015127 (UMLS CUI [1,2])
    Etiologic subtype
    Code List
    For the qualifying stroke, please categories the etiologic subtype below (indicate one only)
    CL Item
    Large-artery atherosclerosis (1)
    CL Item
    Cardioembolism (2)
    CL Item
    Small-artery occlusion (lacune) (3)
    CL Item
    Acute stroke of other determined etiology (4)
    CL Item
    Stroke of underdetermined etiology (5)
    Item Group
    Concomitant Medication
    C2347852 (UMLS CUI-1)
    Medication taken
    Item
    Are any medications listed below currently being taken on the day of visit 1?
    boolean
    C1553892 (UMLS CUI [1])
    Item
    If yes, please indicate which, if any, of the following are currently being taken:
    integer
    C1553892 (UMLS CUI [1])
    If yes, please indicate which
    Code List
    If yes, please indicate which, if any, of the following are currently being taken:
    CL Item
    Dipyridamole (0)
    CL Item
    Aspirin (1)
    CL Item
    Ticlopidine (2)
    CL Item
    Clopidogrel (3)
    CL Item
    Aspirin/extended release Dipyridamole (4)
    CL Item
    Oral anticoagulants (5)
    CL Item
    Nitrates (oral or topical) (6)
    CL Item
    Estrogen replacement without progesterone (7)
    CL Item
    Estrogen replacement with progesterone (8)
    CL Item
    Digitalis (9)
    CL Item
    Statins (10)
    CL Item
    Fibrates (11)
    CL Item
    Dilitazem/Verapamil (12)
    CL Item
    Other calcium channel blockers (13)
    CL Item
    Alpha-blocker (14)
    CL Item
    Direct vasodilators (15)
    CL Item
    Angiotensin Receptor Blocker (ARB) (16)
    CL Item
    Peripheral sympatholytic (17)
    CL Item
    Central sympatholytic (18)
    CL Item
    Alpha-beta blocker (19)
    CL Item
    Beta-blocker (20)
    CL Item
    Loop-active diuretics (21)
    CL Item
    Diuretics of thiazide type (22)
    CL Item
    Potassium-sparing diuretics (23)
    CL Item
    Insulin (24)
    CL Item
    Oral hypoglycemic agents (25)
    CL Item
    Non-steroidal anti-inflammatory drugs (26)
    CL Item
    Specific Cox II inhibitors (27)
    Item Group
    ACE Inhibitors
    C0003015 (UMLS CUI-1)
    ACE Inhibitors currently taken
    Item
    Are ACE Inhibitors currently being taken on the day of visit 1?
    boolean
    C0013227 (UMLS CUI [1])
    Name of ACE Inhibitor and Total Daily Dose
    Item
    Name of ACE Inhibitor 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])
    Retour au début de la page 

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