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ID

25704

Beschreibung

Study ID: 101468/197 Clinical Study ID: SKF-101468/197 Study Title:An open study to compare the PK and tolerability of ropinirole administered as 5 different new formulations with the standard, marketed formulation in healthy volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication : Restless Legs Syndrome

Stichworte

  1. 11.09.17 11.09.17 -
  2. 11.09.17 11.09.17 -
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GlaxoSmithKline

Hochgeladen am

11. September 2017

DOI

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Creative Commons BY-NC 3.0

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    visit period 1,2,3 & 4 cardiovascular monitoring day 1 PK and tolerability of ropinirole as 5 new formulations 101468/197

    visit period 1,2,3 & 4 cardiovascular monitoring day 1 PK and tolerability of ropinirole as 5 new formulations 101468/197

    Administrative Data
    Beschreibung

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Focus Panel ID
    Beschreibung

    focus panel

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C3846158
    Patient No
    Beschreibung

    patient number

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C1830427
    Date
    Beschreibung

    date

    Datentyp

    date

    Alias
    UMLS CUI [1]
    C0011008
    Number of Visit
    Beschreibung

    visit number

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C1549755
    Treatment
    Beschreibung

    treatment

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C0087111
    Cardiovascular Monitoring
    Beschreibung

    Cardiovascular Monitoring

    Alias
    UMLS CUI-1
    C0007226
    Time relative to dosing
    Beschreibung

    time relative to dosing

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0439564
    UMLS CUI [1,2]
    C3469597
    UMLS CUI [1,3]
    C0304229
    Actual Time
    Beschreibung

    actual time

    Datentyp

    time

    Alias
    UMLS CUI [1]
    C0040223
    Semi-supine BP: Systolic
    Beschreibung

    blood pressure systolic in semi-supine position

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0871470
    UMLS CUI [1,2]
    C0038846
    Semi-supine BP: Diastolic
    Beschreibung

    blood pressure diastolic in semi-supine position

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0428883
    UMLS CUI [1,2]
    C0038846
    Semi-supine Bts/min
    Beschreibung

    heart rate in semi-supine position

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0018810
    UMLS CUI [1,2]
    C0038846
    Actual Time
    Beschreibung

    actual time

    Datentyp

    time

    Alias
    UMLS CUI [1]
    C0040223
    Erect BP: Systolic
    Beschreibung

    blood pressure systolic standing

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0871470
    UMLS CUI [1,2]
    C0231472
    Erecet BP: Diastolic
    Beschreibung

    blood pressure diastolic ins standing position

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0428883
    UMLS CUI [1,2]
    C0231472
    Erect pulse Bts/min
    Beschreibung

    heart rate in standing position

    Datentyp

    integer

    Alias
    UMLS CUI [1,1]
    C0018810
    UMLS CUI [1,2]
    C0231472
    Comments
    Beschreibung

    Comments

    Alias
    UMLS CUI-1
    C0947611
    Comments
    Beschreibung

    comments

    Datentyp

    text

    Alias
    UMLS CUI [1]
    C0947611

    Ähnliche Modelle

    visit period 1,2,3 & 4 cardiovascular monitoring day 1 PK and tolerability of ropinirole as 5 new formulations 101468/197

    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    focus panel
    Item
    Focus Panel ID
    integer
    C3846158 (UMLS CUI [1])
    patient number
    Item
    Patient No
    integer
    C1830427 (UMLS CUI [1])
    date
    Item
    Date
    date
    C0011008 (UMLS CUI [1])
    Item
    Number of Visit
    text
    C1549755 (UMLS CUI [1])
    Code List
    Number of Visit
    CL Item
    Period 1 (Period 1)
    CL Item
    Period 2 (Period 2)
    CL Item
    Period 3 (Period 3)
    CL Item
    Period 4 (Period 4)
    treatment
    Item
    Treatment
    text
    C0087111 (UMLS CUI [1])
    Item Group
    Cardiovascular Monitoring
    C0007226 (UMLS CUI-1)
    Item
    Time relative to dosing
    text
    C0439564 (UMLS CUI [1,1])
    C3469597 (UMLS CUI [1,2])
    C0304229 (UMLS CUI [1,3])
    Code List
    Time relative to dosing
    CL Item
    predose (predose)
    CL Item
    +1hr (+1hr)
    CL Item
    +2hrs (+2hrs)
    CL Item
    +3hrs (+3hrs)
    CL Item
    +4hrs (+4hrs)
    CL Item
    +5hrs (+5hrs)
    CL Item
    +6hrs (+6hrs)
    CL Item
    +8hrs (+8hrs)
    CL Item
    +12hrs (+12hrs)
    actual time
    Item
    Actual Time
    time
    C0040223 (UMLS CUI [1])
    blood pressure systolic in semi-supine position
    Item
    Semi-supine BP: Systolic
    integer
    C0871470 (UMLS CUI [1,1])
    C0038846 (UMLS CUI [1,2])
    blood pressure diastolic in semi-supine position
    Item
    Semi-supine BP: Diastolic
    integer
    C0428883 (UMLS CUI [1,1])
    C0038846 (UMLS CUI [1,2])
    heart rate in semi-supine position
    Item
    Semi-supine Bts/min
    integer
    C0018810 (UMLS CUI [1,1])
    C0038846 (UMLS CUI [1,2])
    actual time
    Item
    Actual Time
    time
    C0040223 (UMLS CUI [1])
    blood pressure systolic standing
    Item
    Erect BP: Systolic
    integer
    C0871470 (UMLS CUI [1,1])
    C0231472 (UMLS CUI [1,2])
    blood pressure diastolic ins standing position
    Item
    Erecet BP: Diastolic
    integer
    C0428883 (UMLS CUI [1,1])
    C0231472 (UMLS CUI [1,2])
    heart rate in standing position
    Item
    Erect pulse Bts/min
    integer
    C0018810 (UMLS CUI [1,1])
    C0231472 (UMLS CUI [1,2])
    Item Group
    Comments
    C0947611 (UMLS CUI-1)
    comments
    Item
    Comments
    text
    C0947611 (UMLS CUI [1])

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