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13268

Beschreibung

Study part: Visit V6 (Day 196 + - 14). Effectiveness and tolerance of sublingual desensitization with LAIS grass tablets in Patients with an allergic rhinoconjunctivitis caused by grass pollen. A prospective, multi-center, doubleblind, randomized, placebo-controlled Phase III study. Principal Investigator Prof. Dr. med. Ralph Mösges.

Stichworte

  1. 28.01.16 28.01.16 -
  2. 27.09.21 27.09.21 -
Hochgeladen am

28. Januar 2016

DOI

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Creative Commons BY-NC 3.0

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    Visit V6_LAIS grass tablets by allergic rhinoconjunctivitis_EudraCT-Nr.2012-004916-79

    Visit V6 (Day 196 + - 14)

    Visit 6
    Beschreibung

    Visit 6

    Alias
    UMLS CUI-1
    C0545082
    Date of visit
    Beschreibung

    date

    Datentyp

    date

    Alias
    UMLS CUI [1]
    C0011008
    Does the patient still take part in the study?
    Beschreibung

    Study Subject Participation Status

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C2348568
    Did the patient take the medication according to the protocol?
    Beschreibung

    compliance

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C1321605
    If the compliance was not always, please mention in detail
    Beschreibung

    details compliance

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0392360
    UMLS CUI [1,2]
    C1321605
    Comorbidity? Please fill up the form "Documentation adverse event"
    Beschreibung

    Comorbidity

    Datentyp

    boolean

    Concomitant medication? Please use the form "Documentation Concomitant medication"
    Beschreibung

    Concomitant medication

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C2347852
    Date for next visit 7 (Day 238 + - 14 days)
    Beschreibung

    Date

    Datentyp

    date

    Alias
    UMLS CUI [1]
    C0011008
    Did an adverse event occur during the treatment? (If yes, please use the form "Documentation adverse event")
    Beschreibung

    adverse event

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0877248
    Did a serious adverse event occur during the treatment? (If yes, please use the form "Documentation serious adverse events")
    Beschreibung

    serious adverse event

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C1519255
    Are there any undocumented adverse events, which were not recorded during the previous visit? (If yes, please use the form "Documentation adverse event")
    Beschreibung

    adverse event

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C0877248
    Patient diary part 1 collected and part 2 handed out?
    Beschreibung

    To document daily symptoms and the use of concomitant medication

    Datentyp

    boolean

    Alias
    UMLS CUI [1]
    C3890583
    Did the patient fill up the documentation forms on quality of life of rhinoconjunctivitis patients and Rhinitis control assessment test?
    Beschreibung

    Quality of life; Rhinoconjunctivitis

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C0034380
    UMLS CUI [2]
    C0861155
    Physical examination
    Beschreibung

    Physical examination

    Alias
    UMLS CUI-1
    C0031809
    Weight
    Beschreibung

    Weight

    Datentyp

    float

    Maßeinheiten
    • kg
    Alias
    UMLS CUI [1]
    C0005910
    kg
    Systolic blood pressure
    Beschreibung

    systolic blood pressure

    Datentyp

    integer

    Maßeinheiten
    • mmHg
    Alias
    UMLS CUI [1]
    C0871470
    mmHg
    Diastolic blood pressure
    Beschreibung

    Diastolic blood pressure

    Datentyp

    integer

    Maßeinheiten
    • mmHg
    Alias
    UMLS CUI [1]
    C0428883
    mmHg
    Heart rate
    Beschreibung

    heart rate

    Datentyp

    integer

    Maßeinheiten
    • 1/ min
    Alias
    UMLS CUI [1]
    C0018810
    1/ min
    Examination (Rhinoscope)
    Beschreibung

    Examination (Rhinoscope)

    Alias
    UMLS CUI-1
    C0582103
    UMLS CUI-2
    C0183044
    Edema
    Beschreibung

    edema

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C0013604
    Secretion
    Beschreibung

    Secretion, Nasal

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C1546724
    Redness
    Beschreibung

    Redness

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C0332575
    Spirometry or Peak expiratory flow measurement (For asthmatics)
    Beschreibung

    Spirometry or Peak expiratory flow measurement (For asthmatics)

    Alias
    UMLS CUI-1
    C0037981
    UMLS CUI-3
    C0521299
    FEV1 (age-appropriate standard value)
    Beschreibung

    FEV1

    Datentyp

    float

    Alias
    UMLS CUI [1]
    C0748133
    FEV1
    Beschreibung

    FEV1

    Datentyp

    float

    Alias
    UMLS CUI [1]
    C0748133
    FEV1/ Standard value (If FEV1 < 70% of age appropriate standard value, exclusion)
    Beschreibung

    Ratio; FEV1; standard value

    Datentyp

    integer

    Maßeinheiten
    • %
    Alias
    UMLS CUI [1]
    C0456603
    UMLS CUI [2]
    C0588029
    UMLS CUI [3]
    C1442989
    %
    PEF 1
    Beschreibung

    Peak expiratory flow measurement

    Datentyp

    integer

    Maßeinheiten
    • l/min
    Alias
    UMLS CUI [1]
    C0521299
    l/min
    PEF 2
    Beschreibung

    Peak expiratory flow measurement

    Datentyp

    integer

    Maßeinheiten
    • l/ min
    Alias
    UMLS CUI [1]
    C0521299
    l/ min
    PEF 3
    Beschreibung

    Peak expiratory flow measurement

    Datentyp

    integer

    Maßeinheiten
    • l/ min
    Alias
    UMLS CUI [1]
    C0521299
    l/ min
    Best PEF
    Beschreibung

    Peak expiratory flow measurement

    Datentyp

    integer

    Maßeinheiten
    • l/ min
    Alias
    UMLS CUI [1]
    C0521299
    l/ min
    Optimum individual value PEF (If FEV1 < 70% of optimum individual value, exclusion)
    Beschreibung

    Peak expiratory flow measurement

    Datentyp

    integer

    Maßeinheiten
    • l/ min
    Alias
    UMLS CUI [1]
    C0521299
    l/ min
    Demand medication
    Beschreibung

    Demand medication

    Alias
    UMLS CUI-1
    C0013227
    UMLS CUI-2
    C0441516
    Number of used antihistamines (oral), please specify if incomplete
    Beschreibung

    Antihistamines

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C0003360
    Return of unused medications
    Beschreibung

    medication Demand

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0441516
    Number of opened eyedrops (Levocabastin), please specify if incomplete
    Beschreibung

    Levocabastin

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C0064870
    Return of unused medications
    Beschreibung

    medication Demand

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0441516
    Number of nasal spray bottles opened (Beclometason), please specify if incomplete
    Beschreibung

    Beclometason

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C0004905
    Return of unused medications
    Beschreibung

    medication Demand

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0441516
    Number of opened packets of combination of inhaled cortisone + long acting β2-receptor-agonist, please specify if incomplete
    Beschreibung

    cortisone; beta agonist

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C0010137
    UMLS CUI [2]
    C0001644
    Return of unused medications
    Beschreibung

    medication Demand

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0013227
    UMLS CUI [1,2]
    C0441516

    Ähnliche Modelle

    Visit V6 (Day 196 + - 14)

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    Visit 6
    C0545082 (UMLS CUI-1)
    date
    Item
    Date of visit
    date
    C0011008 (UMLS CUI [1])
    Item
    Does the patient still take part in the study?
    text
    C2348568 (UMLS CUI [1])
    Code List
    Does the patient still take part in the study?
    CL Item
    yes (1)
    CL Item
    no, please then fill up the form "Study completion" (2)
    Item
    Did the patient take the medication according to the protocol?
    text
    C1321605 (UMLS CUI [1])
    Code List
    Did the patient take the medication according to the protocol?
    CL Item
    always (1)
    CL Item
    mostly yes (2)
    CL Item
    mostly no (3)
    CL Item
    no (4)
    details compliance
    Item
    If the compliance was not always, please mention in detail
    text
    C0392360 (UMLS CUI [1,1])
    C1321605 (UMLS CUI [1,2])
    Comorbidity
    Item
    Comorbidity? Please fill up the form "Documentation adverse event"
    boolean
    Concomitant medication
    Item
    Concomitant medication? Please use the form "Documentation Concomitant medication"
    boolean
    C2347852 (UMLS CUI [1])
    Date
    Item
    Date for next visit 7 (Day 238 + - 14 days)
    date
    C0011008 (UMLS CUI [1])
    adverse event
    Item
    Did an adverse event occur during the treatment? (If yes, please use the form "Documentation adverse event")
    boolean
    C0877248 (UMLS CUI [1])
    serious adverse event
    Item
    Did a serious adverse event occur during the treatment? (If yes, please use the form "Documentation serious adverse events")
    boolean
    C1519255 (UMLS CUI [1])
    adverse event
    Item
    Are there any undocumented adverse events, which were not recorded during the previous visit? (If yes, please use the form "Documentation adverse event")
    boolean
    C0877248 (UMLS CUI [1])
    Patient diary
    Item
    Patient diary part 1 collected and part 2 handed out?
    boolean
    C3890583 (UMLS CUI [1])
    Quality of life; Rhinoconjunctivitis
    Item
    Did the patient fill up the documentation forms on quality of life of rhinoconjunctivitis patients and Rhinitis control assessment test?
    text
    C0034380 (UMLS CUI [1])
    C0861155 (UMLS CUI [2])
    Item Group
    Physical examination
    C0031809 (UMLS CUI-1)
    Weight
    Item
    Weight
    float
    C0005910 (UMLS CUI [1])
    systolic blood pressure
    Item
    Systolic blood pressure
    integer
    C0871470 (UMLS CUI [1])
    Diastolic blood pressure
    Item
    Diastolic blood pressure
    integer
    C0428883 (UMLS CUI [1])
    heart rate
    Item
    Heart rate
    integer
    C0018810 (UMLS CUI [1])
    Item Group
    Examination (Rhinoscope)
    C0582103 (UMLS CUI-1)
    C0183044 (UMLS CUI-2)
    Item
    Edema
    text
    C0013604 (UMLS CUI [1])
    Code List
    Edema
    CL Item
    no (1)
    CL Item
    slight (2)
    CL Item
    medium (3)
    CL Item
    strong (4)
    Item
    Secretion
    text
    C1546724 (UMLS CUI [1])
    Code List
    Secretion
    CL Item
    no (1)
    CL Item
    slight (2)
    CL Item
    medium (3)
    CL Item
    strong (4)
    Item
    Redness
    text
    C0332575 (UMLS CUI [1])
    Code List
    Redness
    CL Item
    no (1)
    CL Item
    slight (2)
    CL Item
    medium (3)
    CL Item
    strong (4)
    Item Group
    Spirometry or Peak expiratory flow measurement (For asthmatics)
    C0037981 (UMLS CUI-1)
    C0521299 (UMLS CUI-3)
    FEV1
    Item
    FEV1 (age-appropriate standard value)
    float
    C0748133 (UMLS CUI [1])
    FEV1
    Item
    FEV1
    float
    C0748133 (UMLS CUI [1])
    Ratio; FEV1; standard value
    Item
    FEV1/ Standard value (If FEV1 < 70% of age appropriate standard value, exclusion)
    integer
    C0456603 (UMLS CUI [1])
    C0588029 (UMLS CUI [2])
    C1442989 (UMLS CUI [3])
    Peak expiratory flow measurement
    Item
    PEF 1
    integer
    C0521299 (UMLS CUI [1])
    Peak expiratory flow measurement
    Item
    PEF 2
    integer
    C0521299 (UMLS CUI [1])
    Peak expiratory flow measurement
    Item
    PEF 3
    integer
    C0521299 (UMLS CUI [1])
    Peak expiratory flow measurement
    Item
    Best PEF
    integer
    C0521299 (UMLS CUI [1])
    Peak expiratory flow measurement
    Item
    Optimum individual value PEF (If FEV1 < 70% of optimum individual value, exclusion)
    integer
    C0521299 (UMLS CUI [1])
    Item Group
    Demand medication
    C0013227 (UMLS CUI-1)
    C0441516 (UMLS CUI-2)
    Antihistamines
    Item
    Number of used antihistamines (oral), please specify if incomplete
    text
    C0003360 (UMLS CUI [1])
    medication Demand
    Item
    Return of unused medications
    boolean
    C0013227 (UMLS CUI [1,1])
    C0441516 (UMLS CUI [1,2])
    Levocabastin
    Item
    Number of opened eyedrops (Levocabastin), please specify if incomplete
    text
    C0064870 (UMLS CUI [1])
    medication Demand
    Item
    Return of unused medications
    boolean
    C0013227 (UMLS CUI [1,1])
    C0441516 (UMLS CUI [1,2])
    Beclometason
    Item
    Number of nasal spray bottles opened (Beclometason), please specify if incomplete
    text
    C0004905 (UMLS CUI [1])
    medication Demand
    Item
    Return of unused medications
    boolean
    C0013227 (UMLS CUI [1,1])
    C0441516 (UMLS CUI [1,2])
    cortisone; beta agonist
    Item
    Number of opened packets of combination of inhaled cortisone + long acting β2-receptor-agonist, please specify if incomplete
    text
    C0010137 (UMLS CUI [1])
    C0001644 (UMLS CUI [2])
    medication Demand
    Item
    Return of unused medications
    boolean
    C0013227 (UMLS CUI [1,1])
    C0441516 (UMLS CUI [1,2])

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