0 Evaluaciones
ID

37903

Descripción

Study ID: 105036 Clinical Study ID: 105036 Study Title: A single-blind, randomized, placebo-controlled study to investigate the safety, tolerability, and potential effects on betamethasone pharmacokinetics of a co-administered infusion of GSK221149A in healthy female subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: betamethasone Trade Name: Retosiban Study Indication: Women's Health & Pregnancy - Other, pre-term labour

Palabras clave

Versiones (1)
  1. 29/8/19 29/8/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

29 de agosto de 2019

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

  • El más nuevo
  • Más antiguo
  • Popular
  • El más nuevo
    • El más nuevo
    • Más antiguo
    • Popular

    Sin comentarios

    Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

    Betamethasone pharmacokinetics of a co-administered infusion of GSK221149A; 105036

    Inglés

    Study Conclusion

    1 formularios  
    1. StudyEvent: ODM
      1. Study Conclusion
    Study Conclusion
    Descripción

    Study Conclusion

    Alias
    UMLS CUI-1
    C0008976
    UMLS CUI-2
    C1707478
    Date/time of subject completion or withdrawal
    Descripción

    Clinical Trials, Conclusion, Date in time, Time

    Tipo de datos

    datetime

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C1707478
    UMLS CUI [1,3]
    C0011008
    UMLS CUI [1,4]
    C0040223
    Was the subject withdrawn from the study?
    Descripción

    Clinical Trials, Withdraw

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C2349954
    If Yes, specify primary reason for withdrawal
    Descripción

    Clinical Trials, Withdraw, Reason and justification

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C2349954
    UMLS CUI [1,3]
    C0566251
    Specify
    Descripción

    Clinical Trials, Withdraw, Reason and justification

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C2349954
    UMLS CUI [1,3]
    C0566251
    Case book ready for signature
    Descripción

    Clinical Trials, Clinical Study Case, Signature

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C1706256
    UMLS CUI [1,3]
    C1519316
    Office Use 1
    Descripción

    Clinical Trials, Conclusion, Office

    Tipo de datos

    boolean

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C1707478
    UMLS CUI [1,3]
    C0442603
    Office Use 2
    Descripción

    Clinical Trials, Conclusion, Office

    Tipo de datos

    text

    Alias
    UMLS CUI [1,1]
    C0008976
    UMLS CUI [1,2]
    C1707478
    UMLS CUI [1,3]
    C0442603
    Volver a la parte superior de la página

    Similar models

    Study Conclusion

    1 formularios
    1. StudyEvent: ODM
      1. Study Conclusion
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    Alias
    Item Group
    Study Conclusion
    C0008976 (UMLS CUI-1)
    C1707478 (UMLS CUI-2)
    Clinical Trials, Conclusion, Date in time, Time
    Item
    Date/time of subject completion or withdrawal
    datetime
    C0008976 (UMLS CUI [1,1])
    C1707478 (UMLS CUI [1,2])
    C0011008 (UMLS CUI [1,3])
    C0040223 (UMLS CUI [1,4])
    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, specify 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, specify 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 study (4)
    CL Item
    Sponsor terminated study (5)
    CL Item
    Other, specify (6)
    Clinical Trials, Withdraw, Reason and justification
    Item
    Specify
    text
    C0008976 (UMLS CUI [1,1])
    C2349954 (UMLS CUI [1,2])
    C0566251 (UMLS CUI [1,3])
    Clinical Trials, Clinical Study Case, Signature
    Item
    Case book ready for signature
    boolean
    C0008976 (UMLS CUI [1,1])
    C1706256 (UMLS CUI [1,2])
    C1519316 (UMLS CUI [1,3])
    Clinical Trials, Conclusion, Office
    Item
    Office Use 1
    boolean
    C0008976 (UMLS CUI [1,1])
    C1707478 (UMLS CUI [1,2])
    C0442603 (UMLS CUI [1,3])
    Item
    Office Use 2
    text
    C0008976 (UMLS CUI [1,1])
    C1707478 (UMLS CUI [1,2])
    C0442603 (UMLS CUI [1,3])
    Clinical Trials, Conclusion, Office
    Code List
    Office Use 2
    CL Item
    1 (1)
    CL Item
    2 (2)
    CL Item
    3 (3)
    CL Item
    4 (4)
    CL Item
    5 (5)
    CL Item
    6 (6)
    CL Item
    7 (7)
    CL Item
    8 (8)
    CL Item
    9 (9)
    Volver a la parte superior de la página 

    Ayuda

    Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

    Watch Tutorial