ID

4390

Descripción

ODM derived from http://clinicaltrials.gov/show/NCT00895037

Link

http://clinicaltrials.gov/show/NCT00895037

Palabras clave

Versiones (1)
  1. 9/12/13 9/12/13 - Martin Dugas
Subido en

9 de diciembre de 2013

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility NCT00895037 Hemophilia A

Alemán Inglés

Eligibility

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility
Einschlusskriterien
Descripción

Einschlusskriterien

Alias
UMLS CUI 2011AA
CL425202
Patients with hemophilia A of any severity already receiving or starting treatment with ReFacto AF
Descripción

Patients with hemophilia A of any severity already receiving or starting treatment with ReFacto AF

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0272322
SNOMED CT 2011_0131
16872008
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
UMLS CUI 2011AA
C0039798
UMLS CUI 2011AA
C0971600
Ausschlusskriterien
Descripción

Ausschlusskriterien

Alias
UMLS CUI 2011AA
CL425201
Patients with Hemophilia A treated with a product other than Refacto AF
Descripción

Patients with Hemophilia A treated with a product other than Refacto AF

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0019069
SNOMED CT 2011_0131
234440005
MedDRA 14.1
10016080
ICD-10-CM Version 2010
D66
ICD-9-CM Version 2011
286.0
UMLS CUI 2011AA
CL415147
UMLS CUI 2011AA
C1514468
UMLS CUI 2011AA
CL411789
UMLS CUI 2011AA
C0971600
Volver a la parte superior de la página

Similar models

Eligibility

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Einschlusskriterien
CL425202 (UMLS CUI 2011AA)
Patients with hemophilia A of any severity already receiving or starting treatment with ReFacto AF
Item
Patients with hemophilia A of any severity already receiving or starting treatment with ReFacto AF
boolean
C0272322 (UMLS CUI 2011AA)
16872008 (SNOMED CT 2011_0131)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0039798 (UMLS CUI 2011AA)
C0971600 (UMLS CUI 2011AA)
Item Group
Ausschlusskriterien
CL425201 (UMLS CUI 2011AA)
Patients with Hemophilia A treated with a product other than Refacto AF
Item
Patients with Hemophilia A treated with a product other than Refacto AF
boolean
C0019069 (UMLS CUI 2011AA)
234440005 (SNOMED CT 2011_0131)
10016080 (MedDRA 14.1)
D66 (ICD-10-CM Version 2010)
286.0 (ICD-9-CM Version 2011)
CL415147 (UMLS CUI 2011AA)
C1514468 (UMLS CUI 2011AA)
CL411789 (UMLS CUI 2011AA)
C0971600 (UMLS CUI 2011AA)
Volver a la parte superior de la página 

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