ID

13821

Descripción

This study evaluates the effectiveness and safety of MFNS in improving the Treatment of Chronic Sinusitis. ODM derived from:"Randomized Double-blind Clinical Trial on the Efficacy and Safety of 200 mcg BID Mometasone Furoate Nasal Spray (MFNS) or Placebo in the Treatment of Chronic Sinusitis". Leader of the clinical trial: Prof. Dr. med. Karl Hörmann Direktor der Hals-Nasen-Ohren-Klinik / Clinic Director Ear, Nose and Throat Clinic Medical Faculty Mannheim Heidelberg University at the University Medical Centre Mannheim Theodor-Kutzer-Ufer 1-3 68167 Mannheim

Palabras clave

Versiones (1)
  1. 8/3/16 8/3/16 -
Subido en

8 de marzo 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.

Visit 2 - Clinical Trial on the Efficacy and Safety BID Mometasone Furoate Nasal Spray (MFNS) in the Treatment of Chronic Sinusitis

Inglés

Visit 2

1 formularios  
  1. StudyEvent: ODM
    1. Visit 2
Header module
Descripción

Header module

Visit Number
Descripción

Visit Number

Tipo de datos

integer

Alias
UMLS CUI [1]
C1549755
Patient Name
Descripción

Patient Name

Tipo de datos

integer

Alias
UMLS CUI [1]
C1299487
Center #
Descripción

Center #

Tipo de datos

integer

Alias
UMLS CUI [1]
C0009469
Date
Descripción

Date

Tipo de datos

integer

Alias
UMLS CUI [1]
C0011008
Examination
Descripción

Examination

Temperature
Descripción

Body Temperature

Tipo de datos

integer

Unidades de medida
  • °C
Alias
UMLS CUI [1]
C0005903
°C
Blood pressure
Descripción

Blood pressure

Tipo de datos

integer

Alias
UMLS CUI [1]
C0005823
Heart rate
Descripción

Heart rate

Tipo de datos

integer

Unidades de medida
  • 1/sec
Alias
UMLS CUI [1]
C0018810
1/sec
Examination of nose
Descripción

Examination of nose

Tipo de datos

integer

Alias
UMLS CUI [1]
C0558826
Change of sinusitis since last visit
Descripción

Change of sinusitis since last visit

Tipo de datos

integer

Alias
UMLS CUI [1]
C0037199
Were Antibiotics administered?
Descripción

Please state name and type administered

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003232
Endoscopy
Descripción

Endoscopy

Tipo de datos

integer

Alias
UMLS CUI [1]
C0014245
Endoscopy findings
Descripción

Please state if the following symptoms have been detected, please also indicate left and right.

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0014245
UMLS CUI [1,2]
C0243095
Urine pregnancy test
Descripción

Urine pregnancy test

Tipo de datos

integer

Alias
UMLS CUI [1]
C0430056
Dairy
Descripción

Has the patient´s dairy been checked?

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0376660
Concomitant drug
Descripción

Concomitant drug

Concomitant drug
Descripción

Please insert here all drugs, that the patient is taking during this trial and those drugs with dosage adaptation.

Tipo de datos

integer

Alias
UMLS CUI [1]
C2347852
PRN Medicine
Descripción

PRN Medicine

PRN medicine
Descripción

PRN medicine

Tipo de datos

integer

Alias
UMLS CUI [1]
C3166225
Non-drug therapy
Descripción

Non-drug therapy

Tipo de datos

integer

Adverse event
Descripción

Adverse event

Did an adverse event occur?
Descripción

Did an adverse event occur?

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0877248
Is this a serious adverse event
Descripción

Is this a serious adverse event

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1519255
Adverse event form
Descripción

Adverse event form

Tipo de datos

integer

Alias
UMLS CUI [1]
C0877248
Countermeasures, progress,assessment and outcome of AE
Descripción

Countermeasures, progress,assessment and outcome of AE

Tipo de datos

integer

Alias
UMLS CUI [1]
C1705586
Did a serious adverse event occur during the treatment?
Descripción

(If yes, please uinform study director immediately)

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1519255
Volver a la parte superior de la página

Similar models

Visit 2

1 formularios
  1. StudyEvent: ODM
    1. Visit 2
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Header module
Visit Number
Item
Visit Number
integer
C1549755 (UMLS CUI [1])
Patient Name
Item
Patient Name
integer
C1299487 (UMLS CUI [1])
Center #
Item
Center #
integer
C0009469 (UMLS CUI [1])
Date
Item
Date
integer
C0011008 (UMLS CUI [1])
Item Group
Examination
Body Temperature
Item
Temperature
integer
C0005903 (UMLS CUI [1])
Item
Blood pressure
integer
C0005823 (UMLS CUI [1])
Blood pressure
Code List
Blood pressure
CL Item
Systolic (1)
C0871470 (UMLS CUI-1)
CL Item
Diastolic (2)
C0428883 (UMLS CUI-1)
Heart rate
Item
Heart rate
integer
C0018810 (UMLS CUI [1])
Item
Examination of nose
integer
C0558826 (UMLS CUI [1])
Examination of nose
Code List
Examination of nose
CL Item
Done (1)
CL Item
Note done (2)
CL Item
Finding (3)
C0243095 (UMLS CUI-1)
Item
Change of sinusitis since last visit
integer
C0037199 (UMLS CUI [1])
Change of sinusitis since last visit
Code List
Change of sinusitis since last visit
CL Item
Yes (1)
CL Item
No (2)
CL Item
If yes, please specify (3)
Were Antibiotics administered?
Item
Were Antibiotics administered?
boolean
C0003232 (UMLS CUI [1])
Item
Endoscopy
integer
C0014245 (UMLS CUI [1])
Endoscopy
Code List
Endoscopy
CL Item
Done (1)
CL Item
Note done (2)
CL Item
Findings (3)
C0243095 (UMLS CUI-1)
Item
Endoscopy findings
integer
C0014245 (UMLS CUI [1,1])
C0243095 (UMLS CUI [1,2])
Endoscopy findings
Code List
Endoscopy findings
CL Item
edema (1)
C0013604 (UMLS CUI-1)
CL Item
flow of secretion (2)
C0036536 (UMLS CUI-1)
CL Item
irritation  (3)
C1706307 (UMLS CUI-1)
CL Item
ulceration (4)
C0041582 (UMLS CUI-1)
Item
Urine pregnancy test
integer
C0430056 (UMLS CUI [1])
Urine pregnancy test
Code List
Urine pregnancy test
CL Item
Result (1)
Dairy
Item
Dairy
boolean
C0376660 (UMLS CUI [1])
Item Group
Concomitant drug
Item
Concomitant drug
integer
C2347852 (UMLS CUI [1])
Concomitant drug
Code List
Concomitant drug
CL Item
Drug name (1)
C0013227 (UMLS CUI-1)
CL Item
Dosage (2)
C0178602 (UMLS CUI-1)
CL Item
Start of medication (3)
C0451613 (UMLS CUI-1)
CL Item
End of medication (4)
C2826659 (UMLS CUI-1)
CL Item
Indication (5)
C3146298 (UMLS CUI-1)
Item Group
PRN Medicine
Item
PRN medicine
integer
C3166225 (UMLS CUI [1])
PRN medicine
Code List
PRN medicine
CL Item
Drug (1)
C0013227 (UMLS CUI-1)
CL Item
Dosage (2)
C0178602 (UMLS CUI-1)
CL Item
Date (3)
C0011008 (UMLS CUI-1)
CL Item
Indication (4)
C3146298 (UMLS CUI-1)
Item
Non-drug therapy
integer
Non-drug therapy
Code List
Non-drug therapy
CL Item
Typ of treatment (1)
CL Item
Start (2)
CL Item
End (3)
CL Item
Indication (4)
Item Group
Adverse event
Did an adverse event occur?
Item
Did an adverse event occur?
boolean
C0877248 (UMLS CUI [1])
Is this a serious adverse event
Item
Is this a serious adverse event
boolean
C1519255 (UMLS CUI [1])
Item
Adverse event form
integer
C0877248 (UMLS CUI [1])
Adverse event form
Code List
Adverse event form
CL Item
Description of adverse event icd (1)
C1632372 (UMLS CUI-1)
CL Item
Date and time of adverse event (2)
C2826793 (UMLS CUI-1)
CL Item
Previously in CRF documted (3)
CL Item
Progress (4)
C1335499 (UMLS CUI-1)
CL Item
Related to study drug? (5)
C0013175 (UMLS CUI-1)
Countermeasures, progress,assessment and outcome of AE
Item
Countermeasures, progress,assessment and outcome of AE
integer
C1705586 (UMLS CUI [1])
serious adverse event
Item
Did a serious adverse event occur during the treatment?
boolean
C1519255 (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