ID

44609

Descripción

Study part: Visit V6 (Day 196 + - 14). Effectiveness and tolerance of sublingual desensitization with LAIS grass tablets in Patients with an allergic rhinoconjunctivitis caused by grass pollen. A prospective, multi-center, doubleblind, randomized, placebo-controlled Phase III study. Principal Investigator Prof. Dr. med. Ralph Mösges.

Palabras clave

Versiones (2)
  1. 28/1/16 28/1/16 -
  2. 27/9/21 27/9/21 -
Subido en

27 de septiembre de 2021

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.

Visit V6_LAIS grass tablets by allergic rhinoconjunctivitis_EudraCT-Nr.2012-004916-79

Inglés

Visit V6 (Day 196 + - 14)

1 formularios  
Visit 6
Descripción

Visit 6

Alias
UMLS CUI-1
C0545082
Date of visit
Descripción

date

Tipo de datos

date

Alias
UMLS CUI [1]
C0011008
Does the patient still take part in the study?
Descripción

Study Subject Participation Status

Tipo de datos

text

Alias
UMLS CUI [1]
C2348568
Did the patient take the medication according to the protocol?
Descripción

compliance

Tipo de datos

text

Alias
UMLS CUI [1]
C1321605
If the compliance was not always, please mention in detail
Descripción

details compliance

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C1321605
Comorbidity? Please fill up the form "Documentation adverse event"
Descripción

Comorbidity

Tipo de datos

boolean

Concomitant medication? Please use the form "Documentation Concomitant medication"
Descripción

Concomitant medication

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2347852
Date for next visit 7 (Day 238 + - 14 days)
Descripción

Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0011008
Did an adverse event occur during the treatment? (If yes, please use the form "Documentation adverse event")
Descripción

adverse event

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0877248
Did a serious adverse event occur during the treatment? (If yes, please use the form "Documentation serious adverse events")
Descripción

serious adverse event

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1519255
Are there any undocumented adverse events, which were not recorded during the previous visit? (If yes, please use the form "Documentation adverse event")
Descripción

adverse event

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0877248
Patient diary part 1 collected and part 2 handed out?
Descripción

To document daily symptoms and the use of concomitant medication

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3890583
Did the patient fill up the documentation forms on quality of life of rhinoconjunctivitis patients and Rhinitis control assessment test?
Descripción

Quality of life; Rhinoconjunctivitis

Tipo de datos

text

Alias
UMLS CUI [1]
C0034380
UMLS CUI [2]
C0861155
Physical examination
Descripción

Physical examination

Alias
UMLS CUI-1
C0031809
Weight
Descripción

Weight

Tipo de datos

float

Unidades de medida
  • kg
Alias
UMLS CUI [1]
C0005910
kg
Systolic blood pressure
Descripción

systolic blood pressure

Tipo de datos

integer

Unidades de medida
  • mmHg
Alias
UMLS CUI [1]
C0871470
mmHg
Diastolic blood pressure
Descripción

Diastolic blood pressure

Tipo de datos

integer

Unidades de medida
  • mmHg
Alias
UMLS CUI [1]
C0428883
mmHg
Heart rate
Descripción

heart rate

Tipo de datos

integer

Unidades de medida
  • 1/ min
Alias
UMLS CUI [1]
C0018810
1/ min
Examination (Rhinoscope)
Descripción

Examination (Rhinoscope)

Alias
UMLS CUI-1
C0582103
UMLS CUI-2
C0183044
Edema
Descripción

edema

Tipo de datos

text

Alias
UMLS CUI [1]
C0013604
Secretion
Descripción

Secretion, Nasal

Tipo de datos

text

Alias
UMLS CUI [1]
C1546724
Redness
Descripción

Redness

Tipo de datos

text

Alias
UMLS CUI [1]
C0332575
Spirometry or Peak expiratory flow measurement (For asthmatics)
Descripción

Spirometry or Peak expiratory flow measurement (For asthmatics)

Alias
UMLS CUI-1
C0037981
UMLS CUI-3
C0521299
FEV1 (age-appropriate standard value)
Descripción

FEV1

Tipo de datos

float

Alias
UMLS CUI [1]
C0748133
FEV1
Descripción

FEV1

Tipo de datos

float

Alias
UMLS CUI [1]
C0748133
FEV1/ Standard value (If FEV1 < 70% of age appropriate standard value, exclusion)
Descripción

Ratio; FEV1; standard value

Tipo de datos

integer

Unidades de medida
  • %
Alias
UMLS CUI [1]
C0456603
UMLS CUI [2]
C0588029
UMLS CUI [3]
C1442989
%
PEF 1
Descripción

Peak expiratory flow measurement

Tipo de datos

integer

Unidades de medida
  • l/min
Alias
UMLS CUI [1]
C0521299
l/min
PEF 2
Descripción

Peak expiratory flow measurement

Tipo de datos

integer

Unidades de medida
  • l/ min
Alias
UMLS CUI [1]
C0521299
l/ min
PEF 3
Descripción

Peak expiratory flow measurement

Tipo de datos

integer

Unidades de medida
  • l/ min
Alias
UMLS CUI [1]
C0521299
l/ min
Best PEF
Descripción

Peak expiratory flow measurement

Tipo de datos

integer

Unidades de medida
  • l/ min
Alias
UMLS CUI [1]
C0521299
l/ min
Optimum individual value PEF (If FEV1 < 70% of optimum individual value, exclusion)
Descripción

Peak expiratory flow measurement

Tipo de datos

integer

Unidades de medida
  • l/ min
Alias
UMLS CUI [1]
C0521299
l/ min
Demand medication
Descripción

Demand medication

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0441516
Number of used antihistamines (oral), please specify if incomplete
Descripción

Antihistamines

Tipo de datos

text

Alias
UMLS CUI [1]
C0019590
Return of unused medications
Descripción

medication Demand

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0441516
Number of opened eyedrops (Levocabastin), please specify if incomplete
Descripción

Levocabastin

Tipo de datos

text

Alias
UMLS CUI [1]
C0064870
Return of unused medications
Descripción

medication Demand

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0441516
Number of nasal spray bottles opened (Beclometason), please specify if incomplete
Descripción

Beclometason

Tipo de datos

text

Alias
UMLS CUI [1]
C0004905
Return of unused medications
Descripción

medication Demand

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0441516
Number of opened packets of combination of inhaled cortisone + long acting β2-receptor-agonist, please specify if incomplete
Descripción

cortisone; beta agonist

Tipo de datos

text

Alias
UMLS CUI [1]
C0010137
UMLS CUI [2]
C0001644
Return of unused medications
Descripción

medication Demand

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0441516
Volver a la parte superior de la página

Similar models

Visit V6 (Day 196 + - 14)

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Visit 6
C0545082 (UMLS CUI-1)
date
Item
Date of visit
date
C0011008 (UMLS CUI [1])
Item
Does the patient still take part in the study?
text
C2348568 (UMLS CUI [1])
Study Subject Participation Status
Code List
Does the patient still take part in the study?
CL Item
yes (1)
CL Item
no, please then fill up the form "Study completion" (2)
Item
Did the patient take the medication according to the protocol?
text
C1321605 (UMLS CUI [1])
compliance
Code List
Did the patient take the medication according to the protocol?
CL Item
always (1)
CL Item
mostly yes (2)
CL Item
mostly no (3)
CL Item
no (4)
details compliance
Item
If the compliance was not always, please mention in detail
text
C0392360 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
Comorbidity
Item
Comorbidity? Please fill up the form "Documentation adverse event"
boolean
Concomitant medication
Item
Concomitant medication? Please use the form "Documentation Concomitant medication"
boolean
C2347852 (UMLS CUI [1])
Date
Item
Date for next visit 7 (Day 238 + - 14 days)
date
C0011008 (UMLS CUI [1])
adverse event
Item
Did an adverse event occur during the treatment? (If yes, please use the form "Documentation adverse event")
boolean
C0877248 (UMLS CUI [1])
serious adverse event
Item
Did a serious adverse event occur during the treatment? (If yes, please use the form "Documentation serious adverse events")
boolean
C1519255 (UMLS CUI [1])
adverse event
Item
Are there any undocumented adverse events, which were not recorded during the previous visit? (If yes, please use the form "Documentation adverse event")
boolean
C0877248 (UMLS CUI [1])
Patient diary
Item
Patient diary part 1 collected and part 2 handed out?
boolean
C3890583 (UMLS CUI [1])
Quality of life; Rhinoconjunctivitis
Item
Did the patient fill up the documentation forms on quality of life of rhinoconjunctivitis patients and Rhinitis control assessment test?
text
C0034380 (UMLS CUI [1])
C0861155 (UMLS CUI [2])
Item Group
Physical examination
C0031809 (UMLS CUI-1)
Weight
Item
Weight
float
C0005910 (UMLS CUI [1])
systolic blood pressure
Item
Systolic blood pressure
integer
C0871470 (UMLS CUI [1])
Diastolic blood pressure
Item
Diastolic blood pressure
integer
C0428883 (UMLS CUI [1])
heart rate
Item
Heart rate
integer
C0018810 (UMLS CUI [1])
Item Group
Examination (Rhinoscope)
C0582103 (UMLS CUI-1)
C0183044 (UMLS CUI-2)
Item
Edema
text
C0013604 (UMLS CUI [1])
edema
Code List
Edema
CL Item
no (1)
CL Item
slight (2)
CL Item
medium (3)
CL Item
strong (4)
Item
Secretion
text
C1546724 (UMLS CUI [1])
Secretion, Nasal
Code List
Secretion
CL Item
no (1)
CL Item
slight (2)
CL Item
medium (3)
CL Item
strong (4)
Item
Redness
text
C0332575 (UMLS CUI [1])
Redness
Code List
Redness
CL Item
no (1)
CL Item
slight (2)
CL Item
medium (3)
CL Item
strong (4)
Item Group
Spirometry or Peak expiratory flow measurement (For asthmatics)
C0037981 (UMLS CUI-1)
C0521299 (UMLS CUI-3)
FEV1
Item
FEV1 (age-appropriate standard value)
float
C0748133 (UMLS CUI [1])
FEV1
Item
FEV1
float
C0748133 (UMLS CUI [1])
Ratio; FEV1; standard value
Item
FEV1/ Standard value (If FEV1 < 70% of age appropriate standard value, exclusion)
integer
C0456603 (UMLS CUI [1])
C0588029 (UMLS CUI [2])
C1442989 (UMLS CUI [3])
Peak expiratory flow measurement
Item
PEF 1
integer
C0521299 (UMLS CUI [1])
Peak expiratory flow measurement
Item
PEF 2
integer
C0521299 (UMLS CUI [1])
Peak expiratory flow measurement
Item
PEF 3
integer
C0521299 (UMLS CUI [1])
Peak expiratory flow measurement
Item
Best PEF
integer
C0521299 (UMLS CUI [1])
Peak expiratory flow measurement
Item
Optimum individual value PEF (If FEV1 < 70% of optimum individual value, exclusion)
integer
C0521299 (UMLS CUI [1])
Item Group
Demand medication
C0013227 (UMLS CUI-1)
C0441516 (UMLS CUI-2)
Antihistamines
Item
Number of used antihistamines (oral), please specify if incomplete
text
C0019590 (UMLS CUI [1])
medication Demand
Item
Return of unused medications
boolean
C0013227 (UMLS CUI [1,1])
C0441516 (UMLS CUI [1,2])
Levocabastin
Item
Number of opened eyedrops (Levocabastin), please specify if incomplete
text
C0064870 (UMLS CUI [1])
medication Demand
Item
Return of unused medications
boolean
C0013227 (UMLS CUI [1,1])
C0441516 (UMLS CUI [1,2])
Beclometason
Item
Number of nasal spray bottles opened (Beclometason), please specify if incomplete
text
C0004905 (UMLS CUI [1])
medication Demand
Item
Return of unused medications
boolean
C0013227 (UMLS CUI [1,1])
C0441516 (UMLS CUI [1,2])
cortisone; beta agonist
Item
Number of opened packets of combination of inhaled cortisone + long acting β2-receptor-agonist, please specify if incomplete
text
C0010137 (UMLS CUI [1])
C0001644 (UMLS CUI [2])
medication Demand
Item
Return of unused medications
boolean
C0013227 (UMLS CUI [1,1])
C0441516 (UMLS CUI [1,2])
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