ID

15674

Descripción

Nerventra Study (Eudra CT 2007-003226-19) Study MS-LAQ-301: A multinational, multicenter, randomized, double-blind, parallel-group, placebo-controlled study, to evaluate the safety, tolerability and efficacy of daily oral administration of laquinimod 0.6 mg in subjects with relapsing remitting multiple sclerosis (RRMS)

Palabras clave

Versiones (1)
  1. 8/6/16 8/6/16 -
Subido en

8 de junio de 2016

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.

Nerventra Study Visit 6

Inglés

Nerventra Study Visit 6

1 formularios  
Demographic Information Visit 3
Descripción

Demographic Information Visit 3

Protocol Number
Descripción

Protocol Number

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0008971
UMLS CUI [1,2]
C0600091
Visit Type
Descripción

i.e "Screening"

Tipo de datos

text

Alias
UMLS CUI [1]
C0545082
Date of visit
Descripción

Visit date

Tipo de datos

date

Alias
UMLS CUI [1]
C1320303
Study site number
Descripción

Study site

Tipo de datos

integer

Alias
UMLS CUI [1]
C2825164
Subject number:
Descripción

Subject number

Tipo de datos

integer

Alias
UMLS CUI [1]
C1709561
Section blank?
Descripción

Blank

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0750479
Repeated MRI Scan Performance Visit 6
Descripción

Repeated MRI Scan Performance Visit 6

Date of MRI
Descripción

date MRI

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0024485
MRI not done
Descripción

MRI

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0024485
Type of Gadolinium-based contrast agent used
Descripción

Contrast agent

Tipo de datos

integer

Alias
UMLS CUI [1]
C0009924
Other contrast agent used
Descripción

Contrast agent

Tipo de datos

text

Alias
UMLS CUI [1]
C0009924
Was MRI completed according to the protocol?
Descripción

MRI performed

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0024485
Reason MRI was not completed
Descripción

MRI

Tipo de datos

text

Alias
UMLS CUI [1]
C0024485
Where there any pathological,non-MS findings?
Descripción

Findings

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0243095
Please specify pathological findings
Descripción

If an adverse event occurs during the MRI performance, please inform the investigator in order to record on adverse event log

Tipo de datos

text

Alias
UMLS CUI [1]
C0243095
Volver a la parte superior de la página

Similar models

Nerventra Study Visit 6

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Demographic Information Visit 3
Protocol Number
Item
Protocol Number
text
C0008971 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Visit
Item
Visit Type
text
C0545082 (UMLS CUI [1])
Visit date
Item
Date of visit
date
C1320303 (UMLS CUI [1])
Study site
Item
Study site number
integer
C2825164 (UMLS CUI [1])
Subject number
Item
Subject number:
integer
C1709561 (UMLS CUI [1])
Blank
Item
Section blank?
boolean
C0750479 (UMLS CUI [1])
Item Group
Repeated MRI Scan Performance Visit 6
date MRI
Item
Date of MRI
date
C0011008 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
MRI
Item
MRI not done
boolean
C0024485 (UMLS CUI [1])
Item
Type of Gadolinium-based contrast agent used
integer
C0009924 (UMLS CUI [1])
Contrast agent
Code List
Type of Gadolinium-based contrast agent used
CL Item
Magnevist (1)
CL Item
Omniscan (2)
CL Item
Dotarem (3)
CL Item
Other (specify) (4)
Contrast agent
Item
Other contrast agent used
text
C0009924 (UMLS CUI [1])
MRI performed
Item
Was MRI completed according to the protocol?
boolean
C0024485 (UMLS CUI [1])
MRI
Item
Reason MRI was not completed
text
C0024485 (UMLS CUI [1])
Findings
Item
Where there any pathological,non-MS findings?
boolean
C0243095 (UMLS CUI [1])
Findings
Item
Please specify pathological findings
text
C0243095 (UMLS CUI [1])
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