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ID

12578

Beschreibung

Neutrophil Gelatinase-Associated Lipcalin (NGAL) Evaluation Along With B-Type Natriuretic Peptide in Acutely Decompensated HF; ODM derived from: https://clinicaltrials.gov/show/NCT00693745

Link

https://clinicaltrials.gov/show/NCT00693745

Stichworte

  1. 02.12.15 02.12.15 -
Hochgeladen am

2. Dezember 2015

DOI

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Lizenz

Creative Commons BY 4.0

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    Eligibility Acute Decompensated Heart Failure NCT00693745

    Eligibility Acute Decompensated Heart Failure NCT00693745

    Inclusion Criteria
    Beschreibung

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    male or female 18 years of age or older.
    Beschreibung

    Patient sex and age

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0150831
    UMLS CUI [1,2]
    C0001779
    patients presenting to the emergency department / hospital with symptoms of new or decompensated heart failure and who will be treated with at least one dose of iv diuretic;
    Beschreibung

    patients presenting to the emergency department / hospital with symptoms of new or decompensated heart failure and who will be treated with at least one dose of iv diuretic

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0562508
    UMLS CUI [2]
    C0581377
    UMLS CUI [3]
    C3898697
    ability to draw blood samples for baseline ngal, bnp and creatinine levels either prior to the administration of the first dose of iv diuretic or within 1 hour after the first dose of an iv diuretic
    Beschreibung

    blood samples for baseline ngal, bnp and creatinine levels

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0190979
    UMLS CUI [2]
    C0748313
    ability to provide written informed consent from subject or their authorized representative.
    Beschreibung

    informed consent

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Beschreibung

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    acute myocardial infarction or active ischemia ;
    Beschreibung

    acute myocardial infarction or active ischemia

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0155626
    UMLS CUI [2]
    C0151744
    patients who are intubated or otherwise not able to communicate or comply with study assessments
    Beschreibung

    patients who are intubated or otherwise not able to communicate or comply with study assessments

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0525058
    UMLS CUI [2]
    C0439801
    UMLS CUI [3]
    C0009488
    cardiogenic shock or any other clinical condition that would contraindicate the administration of an iv agent with potent vasodilating properties
    Beschreibung

    cardiogenic shock or any other clinical condition that would contraindicate the administration of an iv agent with potent vasodilating properties

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0525058
    UMLS CUI [2]
    C0439801
    UMLS CUI [3]
    C0009488
    known history of marked renal insufficiency (e.g., usual serum creatinine ≥ 3.0 mg/dl), on dialysis (either acute of chronic) or in imminent need of dialysis at enrollment;
    Beschreibung

    marked renal insufficiency, on dialysis or in imminent need of dialysis

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1536070
    UMLS CUI [2]
    C0011946
    prisoners or other institutionalized or vulnerable individuals;
    Beschreibung

    vulnerable individuals

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0949366
    participation in an interventional clinical study within the previous 30 days;
    Beschreibung

    participation in another interventional clinical study

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    unlikely to be willing or able to comply with study procedures, including the follow-up at 30 and 90 days .
    Beschreibung

    unlikely to be willing or able to comply with study procedures

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1321605

    Ähnliche Modelle

    Eligibility Acute Decompensated Heart Failure NCT00693745

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Patient sex and age
    Item
    male or female 18 years of age or older.
    boolean
    C0150831 (UMLS CUI [1,1])
    C0001779 (UMLS CUI [1,2])
    patients presenting to the emergency department / hospital with symptoms of new or decompensated heart failure and who will be treated with at least one dose of iv diuretic
    Item
    patients presenting to the emergency department / hospital with symptoms of new or decompensated heart failure and who will be treated with at least one dose of iv diuretic;
    boolean
    C0562508 (UMLS CUI [1])
    C0581377 (UMLS CUI [2])
    C3898697 (UMLS CUI [3])
    blood samples for baseline ngal, bnp and creatinine levels
    Item
    ability to draw blood samples for baseline ngal, bnp and creatinine levels either prior to the administration of the first dose of iv diuretic or within 1 hour after the first dose of an iv diuretic
    boolean
    C0190979 (UMLS CUI [1])
    C0748313 (UMLS CUI [2])
    informed consent
    Item
    ability to provide written informed consent from subject or their authorized representative.
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    acute myocardial infarction or active ischemia
    Item
    acute myocardial infarction or active ischemia ;
    boolean
    C0155626 (UMLS CUI [1])
    C0151744 (UMLS CUI [2])
    patients who are intubated or otherwise not able to communicate or comply with study assessments
    Item
    patients who are intubated or otherwise not able to communicate or comply with study assessments
    boolean
    C0525058 (UMLS CUI [1])
    C0439801 (UMLS CUI [2])
    C0009488 (UMLS CUI [3])
    cardiogenic shock or any other clinical condition that would contraindicate the administration of an iv agent with potent vasodilating properties
    Item
    cardiogenic shock or any other clinical condition that would contraindicate the administration of an iv agent with potent vasodilating properties
    boolean
    C0525058 (UMLS CUI [1])
    C0439801 (UMLS CUI [2])
    C0009488 (UMLS CUI [3])
    marked renal insufficiency, on dialysis or in imminent need of dialysis
    Item
    known history of marked renal insufficiency (e.g., usual serum creatinine ≥ 3.0 mg/dl), on dialysis (either acute of chronic) or in imminent need of dialysis at enrollment;
    boolean
    C1536070 (UMLS CUI [1])
    C0011946 (UMLS CUI [2])
    vulnerable individuals
    Item
    prisoners or other institutionalized or vulnerable individuals;
    boolean
    C0949366 (UMLS CUI [1])
    participation in another interventional clinical study
    Item
    participation in an interventional clinical study within the previous 30 days;
    boolean
    C2348568 (UMLS CUI [1])
    unlikely to be willing or able to comply with study procedures
    Item
    unlikely to be willing or able to comply with study procedures, including the follow-up at 30 and 90 days .
    boolean
    C1321605 (UMLS CUI [1])

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