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ID

39192

Beschreibung

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

Stichworte

Versionen (1)
  1. 08.12.19 08.12.19 -
Rechteinhaber

GlaxoSmithKline

Hochgeladen am

8. Dezember 2019

DOI

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Lizenz

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

    Englisch

    Study Conclusion

    1 Formulare  
    1. StudyEvent: ODM
      1. Study Conclusion
    Administrative Data
    Beschreibung

    Administrative Data

    Alias
    UMLS CUI-1
    C1320722
    Subject Identifier
    Beschreibung

    Clinical Trial Subject Unique Identifier

    Datentyp

    integer

    Alias
    UMLS CUI [1]
    C2348585
    Study Conclusion
    Beschreibung

    Study Conclusion

    Alias
    UMLS CUI-1
    C0008976
    UMLS CUI-2
    C1707478
    Date of subject completion or withdrawal
    Beschreibung

    Clinical Trials, End Date

    Datentyp

    date

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C0806020
    Time of withdrawal
    Beschreibung

    Clinical Trials, Withdraw, Time

    Datentyp

    time

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C2349954
    UMLS CUI [1,3]
    C0040223
    Was the subject withdrawn from the study?
    Beschreibung

    Clinical Trials, Withdraw

    Datentyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C2349954
    If Yes, check the primary reason for withdrawal
    Beschreibung

    Clinical Trials, Withdraw, Reason and justification

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C2349954
    UMLS CUI [1,3]
    C0566251
    Other, specify
    Beschreibung

    Clinical Trials, Withdraw, Reason and justification

    Datentyp

    text

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C2349954
    UMLS CUI [1,3]
    C0566251
    Zum Seitenanfang zurückkehren

    Ähnliche Modelle

    Study Conclusion

    1 Formulare
    1. StudyEvent: ODM
      1. Study Conclusion
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datentyp
    Alias
    Item Group
    Administrative Data
    C1320722 (UMLS CUI-1)
    Clinical Trial Subject Unique Identifier
    Item
    Subject Identifier
    integer
    C2348585 (UMLS CUI [1])
    Item Group
    Study Conclusion
    C0008976 (UMLS CUI-1)
    C1707478 (UMLS CUI-2)
    Clinical Trials, End Date
    Item
    Date of subject completion or withdrawal
    date
    C0008976 (UMLS CUI [1,1])
    C0806020 (UMLS CUI [1,2])
    Clinical Trials, Withdraw, Time
    Item
    Time of withdrawal
    time
    C0008976 (UMLS CUI [1,1])
    C2349954 (UMLS CUI [1,2])
    C0040223 (UMLS CUI [1,3])
    Clinical Trials, Withdraw
    Item
    Was the subject withdrawn from the study?
    boolean
    C0008976 (UMLS CUI [1,1])
    C2349954 (UMLS CUI [1,2])
    Item
    If Yes, check the primary reason for withdrawal
    text
    C0008976 (UMLS CUI [1,1])
    C2349954 (UMLS CUI [1,2])
    C0566251 (UMLS CUI [1,3])
    Clinical Trials, Withdraw, Reason and justification
    Code List
    If Yes, check the primary reason for withdrawal
    CL Item
    Adverse event  (1)
    CL Item
    Lost to follow-up (2)
    CL Item
    Protocol violation (3)
    CL Item
    Subject decided to withdraw from the study  (4)
    CL Item
    Lack of efficacy (5)
    CL Item
    Sponsor terminated study (6)
    CL Item
    Other, specify (7)
    Clinical Trials, Withdraw, Reason and justification
    Item
    Other, specify
    text
    C0008976 (UMLS CUI [1,1])
    C2349954 (UMLS CUI [1,2])
    C0566251 (UMLS CUI [1,3])
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