ID

31431

Descripción

Study ID: 105012 Clinical Study ID: NSS105012 Study Title: Emotional processing in healthy male volunteers treated with GSK424887. A single centre, randomised, double-blind, placebo-controlled parallel group study Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01424384 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GSK424887 Trade Name: Citalopram Study Indication: Depressive Disorder and Anxiety Disorders

Palabras clave

Versiones (1)
  1. 21/8/18 21/8/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

21 de agosto de 2018

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 :

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

Emotional processing in healthy male volunteers treated with GSK424887 NCT01424384

Inglés

Study Conclusion

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

Study Conclusion

Alias
UMLS CUI-1
C1707478
UMLS CUI-2
C0008976
Date of last contact
Descripción

Date last contact

Tipo de datos

date

Alias
UMLS CUI [1]
C0805839
Was the subject withdrawn from the study?
Descripción

Patient withdrawn from trial

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0422727
If subject was withdrawn from the study, date of decision to withdraw
Descripción

Patient withdrawn from trial; Decision; Date in time

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0679006
UMLS CUI [1,3]
C0011008
If subject was withdrawn from study, reason for withdrawal
Descripción

Patient withdrawn from trial; Indication of (contextual qualifier)

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C0392360
If primary reason for withdrawal is investigator discretion, please specify.
Descripción

Patient withdrawn from trial; Indication; Clinical Investigators; Specification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0422727
UMLS CUI [1,2]
C3146298
UMLS CUI [1,3]
C0008961
UMLS CUI [1,4]
C2348235
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
C1707478 (UMLS CUI-1)
C0008976 (UMLS CUI-2)
Date last contact
Item
Date of last contact
date
C0805839 (UMLS CUI [1])
Patient withdrawn from trial
Item
Was the subject withdrawn from the study?
boolean
C0422727 (UMLS CUI [1])
Patient withdrawn from trial; Decision; Date in time
Item
If subject was withdrawn from the study, date of decision to withdraw
date
C0422727 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
If subject was withdrawn from study, reason for withdrawal
integer
C0422727 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Patient withdrawn from trial; Indication of (contextual qualifier)
Code List
If subject was withdrawn from study, reason for withdrawal
CL Item
Adverse Event (Record details on the Non- Serious Adverse Events or Serious Adverse Events forms as appropriate) (1)
CL Item
Protocol deviation (3)
CL Item
Subject reached protocol defined stopping criteria (4)
CL Item
Study closed/ terminated (5)
CL Item
Lost to Follow- up (6)
CL Item
Investigator discretion (Select this reason if none of the other primary reasons are appropriate) (7)
CL Item
Withdrew consent (8)
Patient withdrawn from trial; Indication; Clinical Investigators; Specification
Item
If primary reason for withdrawal is investigator discretion, please specify.
text
C0422727 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

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