0 Beoordelingen
ID

39188

Beschrijving

Study ID: 103106 Clinical Study ID: WXL103106 Study Title:An open-label, 2-period, sequential treatment, 1-way drug interaction study to evaluate the effect of ritonavir on bupropion pharmacokinetics 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: bupropion Trade Name: Wellbutrin,QUOMEM,Elontril,Zyban,ZYNTABAC; Zyban,ZYNTABAC,Wellbutrin,Wellburin,QUOMEM,Prolev,Magerion,Geronplase,Elontril Study Indication: Depressive Disorder

Trefwoorden

Versies (1)
  1. 08-12-19 08-12-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

8 december 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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    Effect of Ritonavir on Bupropion Pharmacokinetics; 103106

    Engels

    Concomitant Medications

    1 Formulieren  
    Administrative Data
    Beschrijving

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Identifier
    Beschrijving

    Clinical Trial Subject Unique Identifier

    Datatype

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Concomitant Medications
    Beschrijving

    Concomitant Medications

    Alias
    UMLS CUI-1
    C2347852
    Were any concomitant medications taken by the subject prior to screening and/or during the study?
    Beschrijving

    Concomitant Agent, During, Clinical Trials

    Datatype

    boolean

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0347984
    UMLS CUI [1,3]
    C0008976
    Drug Name
    Beschrijving

    Concomitant Agent, Medication name

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C2360065
    Unit Dose
    Beschrijving

    Concomitant Agent, Dosage

    Datatype

    integer

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0178602
    Units
    Beschrijving

    Concomitant Agent, Unit of Measure

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C1519795
    Frequency
    Beschrijving

    Concomitant Agent, Frequencies

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0439603
    Route
    Beschrijving

    Concomitant Agent, Drug Administration Routes

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0013153
    Reason for Medication
    Beschrijving

    Concomitant Agent, Reason and justification

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C0013153
    Start Date
    Beschrijving

    Concomitant Medication Start Date

    Datatype

    date

    Alias
    UMLS CUI [1]
    C2826734
    Start Time
    Beschrijving

    Concomitant Agent, Start time

    Datatype

    time

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C1301880
    Taken Prior to Study?
    Beschrijving

    Concomitant Medication Previous Occurrence

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C2826667
    Stop Date
    Beschrijving

    Concomitant Medication End Date

    Datatype

    date

    Alias
    UMLS CUI [1]
    C2826744
    Stop Time
    Beschrijving

    Concomitant Agent, End Time

    Datatype

    time

    Alias
    UMLS CUI [1,1]
    C2347852
    UMLS CUI [1,2]
    C1522314
    Ongoing Medication?
    Beschrijving

    Concomitant Medication Ongoing

    Datatype

    boolean

    Alias
    UMLS CUI [1]
    C2826666
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    Similar models

    Concomitant Medications

    1 Formulieren
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Clinical Trial Subject Unique Identifier
    Item
    Subject Identifier
    integer
    C2348585 (UMLS CUI [1])
    Item Group
    Concomitant Medications
    C2347852 (UMLS CUI-1)
    Concomitant Agent, During, Clinical Trials
    Item
    Were any concomitant medications taken by the subject prior to screening and/or during the study?
    boolean
    C2347852 (UMLS CUI [1,1])
    C0347984 (UMLS CUI [1,2])
    C0008976 (UMLS CUI [1,3])
    Concomitant Agent, Medication name
    Item
    Drug Name
    text
    C2347852 (UMLS CUI [1,1])
    C2360065 (UMLS CUI [1,2])
    Concomitant Agent, Dosage
    Item
    Unit Dose
    integer
    C2347852 (UMLS CUI [1,1])
    C0178602 (UMLS CUI [1,2])
    Concomitant Agent, Unit of Measure
    Item
    Units
    text
    C2347852 (UMLS CUI [1,1])
    C1519795 (UMLS CUI [1,2])
    Concomitant Agent, Frequencies
    Item
    Frequency
    text
    C2347852 (UMLS CUI [1,1])
    C0439603 (UMLS CUI [1,2])
    Concomitant Agent, Drug Administration Routes
    Item
    Route
    text
    C2347852 (UMLS CUI [1,1])
    C0013153 (UMLS CUI [1,2])
    Concomitant Agent, Reason and justification
    Item
    Reason for Medication
    text
    C2347852 (UMLS CUI [1,1])
    C0013153 (UMLS CUI [1,2])
    Concomitant Medication Start Date
    Item
    Start Date
    date
    C2826734 (UMLS CUI [1])
    Concomitant Agent, Start time
    Item
    Start Time
    time
    C2347852 (UMLS CUI [1,1])
    C1301880 (UMLS CUI [1,2])
    Concomitant Medication Previous Occurrence
    Item
    Taken Prior to Study?
    boolean
    C2826667 (UMLS CUI [1])
    Concomitant Medication End Date
    Item
    Stop Date
    date
    C2826744 (UMLS CUI [1])
    Concomitant Agent, End Time
    Item
    Stop Time
    time
    C2347852 (UMLS CUI [1,1])
    C1522314 (UMLS CUI [1,2])
    Concomitant Medication Ongoing
    Item
    Ongoing Medication?
    boolean
    C2826666 (UMLS CUI [1])
    Terug naar het begin van de pagina 

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