ID

43211

Descripción

ODM derived from http://clinicaltrials.gov/show/NCT00168051

Link

http://clinicaltrials.gov/show/NCT00168051

Palabras clave

  1. 5/12/11 5/12/11 -
  2. 13/4/14 13/4/14 - Julian Varghese
  3. 10/8/14 10/8/14 - Martin Dugas
  4. 20/9/21 20/9/21 -
Subido en

20 de septiembre de 2021

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility NCT00168051 Hemophilia A

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
18 Years to 64 Years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI-1
C0001779
Male
Descripción

Male gender

Tipo de datos

boolean

Alias
UMLS CUI-1
C0086582
Severe hemophilia A
Descripción

Severe hemophilia A

Tipo de datos

boolean

Alias
UMLS CUI-1
C0019069
Previously treated patients with at least 150 exposure days to any Factor VIII product
Descripción

Treatment with Factor VIII

Tipo de datos

boolean

Alias
UMLS CUI-1
C0087111
UMLS CUI-2
C0015506
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Hypersensitivity to any recombinant Factor VIII product
Descripción

Hypersensitivity Factor VIII

Tipo de datos

boolean

Alias
UMLS CUI-1
C0020517
UMLS CUI-2
C0015506
History of or current Factor VIII inhibitor
Descripción

Factor VIII inhibitor

Tipo de datos

boolean

Alias
UMLS CUI-1
C0368953
Bleeding episode or other reason requiring Factor VIII treatment within 3 days of study
Descripción

Bleeding episode

Tipo de datos

boolean

Alias
UMLS CUI-1
C0005779

Similar models

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Age
Item
18 Years to 64 Years
boolean
C0001779 (UMLS CUI-1)
Male
Item
Male
boolean
C0086582 (UMLS CUI-1)
Hemophilia A
Item
Severe hemophilia A
boolean
C0019069 (UMLS CUI-1)
Treatment with Factor VIII
Item
Previously treated patients with at least 150 exposure days to any Factor VIII product
boolean
C0087111 (UMLS CUI-1)
C0015506 (UMLS CUI-2)
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Hypersensitivity Factor VIII
Item
Hypersensitivity to any recombinant Factor VIII product
boolean
C0020517 (UMLS CUI-1)
C0015506 (UMLS CUI-2)
Factor VIII inhibitor
Item
History of or current Factor VIII inhibitor
boolean
C0368953 (UMLS CUI-1)
Bleeding episode
Item
Bleeding episode or other reason requiring Factor VIII treatment within 3 days of study
boolean
C0005779 (UMLS CUI-1)

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