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ID

25343

Beschrijving

Study part: Pre- Dose Drug Screening (Urine) Week 1 Day 1. A Single Blind, Parallel Group, Up-titration, Phase 1 Study in Healthy Volunteers to Determine a Starting Dose and Select an Up-titration Regimen for a new Formulation of Ropinirole. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Phase: phase 1. Study Recruitment Status: Completed Generic Name: ropinirole. Trade Name: Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP, Zygara; Zygara, ZIPEREVE, ZEPREVE, Requip Depot, REQUIP, REPREVE, Modutab, ADARTREL. Study Indication : Restless Legs Syndrome. Study ID: 101468/201. Clinical Study ID: 101468/201

Trefwoorden

  1. 01-09-17 01-09-17 -
  2. 21-06-19 21-06-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

1 september 2017

DOI

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Licentie

Creative Commons BY-NC 3.0

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    Pre- Dose Drug Screening (Urine) Week 1 Day 1 Ropinirole Restless Legs Syndrome 101468/201

    Pre- Dose Drug Screening (Urine) Week 1 Day 1

    PRE-DOSE DRUG SCREENING (URINE)
    Beschrijving

    PRE-DOSE DRUG SCREENING (URINE)

    Alias
    UMLS CUI-1
    C0202274
    Subject number
    Beschrijving

    Subject number

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Exact date and time of sampling:
    Beschrijving

    date and time

    Datatype

    datetime

    Alias
    UMLS CUI [1]
    C0011008
    Were there any contra-indicated drugs detected?
    Beschrijving

    contraindication drugs

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C1301624
    UMLS CUI [1,2]
    C0013227
    If yes, type of Drug
    Beschrijving

    drug

    Datatype

    text

    Alias
    UMLS CUI [1]
    C0013227
    Comment
    Beschrijving

    Comment

    Datatype

    text

    Alias
    UMLS CUI [1]
    C0947611

    Similar models

    Pre- Dose Drug Screening (Urine) Week 1 Day 1

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    PRE-DOSE DRUG SCREENING (URINE)
    C0202274 (UMLS CUI-1)
    Subject number
    Item
    Subject number
    integer
    C2348585 (UMLS CUI [1])
    date and time
    Item
    Exact date and time of sampling:
    datetime
    C0011008 (UMLS CUI [1])
    contraindication drugs
    Item
    Were there any contra-indicated drugs detected?
    boolean
    C1301624 (UMLS CUI [1,1])
    C0013227 (UMLS CUI [1,2])
    drug
    Item
    If yes, type of Drug
    text
    C0013227 (UMLS CUI [1])
    Comment
    Item
    Comment
    text
    C0947611 (UMLS CUI [1])

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