0 Evaluaciones
ID

32121

Descripción

Study ID: 106218 Clinical Study ID: TDC106218 Study Title: Study On Bioavailability And Pharmacokinetics Of Various Doses Of Testosterone Administered With And Without Dutasteride  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: testosterone Trade Name: Andropatch,Androderm Study Indication: Hypogonadism, Male

Palabras clave

Versiones (2)
  1. 19/10/18 19/10/18 -
  2. 16/11/18 16/11/18 -
Titular de derechos de autor

GSK group of companies

Subido en

19 de octubre de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0
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    Bioavailability and Pharmacokinetics of Testosterone with/without Dutasteride - 106218

    Inglés

    Study Conclusion Form

    1 formularios  
    1. StudyEvent: ODM
      1. Study Conclusion Form
    Administrative data
    Descripción

    Administrative data

    Subject Identifier
    Descripción

    Subject Identifier

    Tipo de datos

    integer

    Study Conclusion
    Descripción

    Study Conclusion

    Tipo de datos

    text

    Date of subject completion or withdrawal
    Descripción

    Date of subject completion or withdrawal

    Tipo de datos

    date

    Was the subject withdrawn from the study?
    Descripción

    Was the subject withdrawn from the study?

    Tipo de datos

    boolean

    If YES, mark the primary reason for withdrawal:
    Descripción

    If YES, mark the primary reason for withdrawal:

    Tipo de datos

    text

    Volver a la parte superior de la página

    Similar models

    Study Conclusion Form

    1 formularios
    1. StudyEvent: ODM
      1. Study Conclusion Form
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Administrative data
    Subject Identifier
    Item
    Subject Identifier
    integer
    Study Conclusion
    Item
    Study Conclusion
    text
    Date of subject completion or withdrawal
    Item
    Date of subject completion or withdrawal
    date
    Was the subject withdrawn from the study?
    Item
    Was the subject withdrawn from the study?
    boolean
    Item
    If YES, mark the primary reason for withdrawal:
    text
    If YES, mark the primary reason for withdrawal:
    Code List
    If YES, mark the primary reason for withdrawal:
    CL Item
    [1] Adverse event -> Record details on the Non-Serious Adverse Events or Serious Adverse Event pages as appropriate. (1)
    CL Item
    [2] Lost to follow-up (2)
    CL Item
    [3] Protocol violation (3)
    CL Item
    [4] Subject decided to withdraw from the study (4)
    CL Item
    [6] Sponsor terminated study (5)
    CL Item
    [Z] Other, specify______________________________ (6)
    Volver a la parte superior de la página 

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