ID

15612

Beschreibung

Safety and Tolerability of Interferon-Beta-1a and Estroprogestins Association in MS Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00151801

Link

https://clinicaltrials.gov/show/NCT00151801

Stichworte

  1. 05.06.16 05.06.16 -
Hochgeladen am

5. Juni 2016

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT00151801

Eligibility Multiple Sclerosis NCT00151801

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
female patients
Beschreibung

female patients

Datentyp

boolean

Alias
UMLS CUI [1]
C0079399
clinically definite relapsing-remitting ms according to the mcdonald criteria
Beschreibung

relapsing-remitting ms

Datentyp

boolean

Alias
UMLS CUI [1]
C0751967
age between 18-40 y.o.
Beschreibung

age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
edss from 0 to 4.0, inclusive
Beschreibung

edss

Datentyp

boolean

Alias
UMLS CUI [1]
C0451246
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of migraine or thromboembolic events
Beschreibung

migraine or thromboembolic events

Datentyp

boolean

Alias
UMLS CUI [1]
C0149931
UMLS CUI [2]
C0040053
reproductive system disorders
Beschreibung

reproductive system disorders

Datentyp

boolean

Alias
UMLS CUI [1]
C0178829
pregnancy or suspension of pregnancy within 12 months prior to randomisation
Beschreibung

pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
prior use of estroprogestins within the last 3 months prior to randomisation
Beschreibung

estroprogestins

Datentyp

boolean

Alias
UMLS CUI [1]
C0015011
prior use of immunosuppressive drugs within the last 12 months prior to randomisation
Beschreibung

immunosuppressive drugs

Datentyp

boolean

Alias
UMLS CUI [1]
C0021081
prior use of immunomodulating drugs within the last 6 months prior to randomisation
Beschreibung

immunomodulating drugs

Datentyp

boolean

Alias
UMLS CUI [1]
C0005525
prior use of corticosteroids within the last 3 months prior to randomisation
Beschreibung

corticosteroids

Datentyp

boolean

Alias
UMLS CUI [1]
C0001617
have clinical relapse 30 days prior to randomisation
Beschreibung

clinical relapse

Datentyp

boolean

Alias
UMLS CUI [1]
C0856120

Ähnliche Modelle

Eligibility Multiple Sclerosis NCT00151801

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
female patients
Item
female patients
boolean
C0079399 (UMLS CUI [1])
relapsing-remitting ms
Item
clinically definite relapsing-remitting ms according to the mcdonald criteria
boolean
C0751967 (UMLS CUI [1])
age
Item
age between 18-40 y.o.
boolean
C0001779 (UMLS CUI [1])
edss
Item
edss from 0 to 4.0, inclusive
boolean
C0451246 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
migraine or thromboembolic events
Item
history of migraine or thromboembolic events
boolean
C0149931 (UMLS CUI [1])
C0040053 (UMLS CUI [2])
reproductive system disorders
Item
reproductive system disorders
boolean
C0178829 (UMLS CUI [1])
pregnancy
Item
pregnancy or suspension of pregnancy within 12 months prior to randomisation
boolean
C0032961 (UMLS CUI [1])
estroprogestins
Item
prior use of estroprogestins within the last 3 months prior to randomisation
boolean
C0015011 (UMLS CUI [1])
immunosuppressive drugs
Item
prior use of immunosuppressive drugs within the last 12 months prior to randomisation
boolean
C0021081 (UMLS CUI [1])
immunomodulating drugs
Item
prior use of immunomodulating drugs within the last 6 months prior to randomisation
boolean
C0005525 (UMLS CUI [1])
corticosteroids
Item
prior use of corticosteroids within the last 3 months prior to randomisation
boolean
C0001617 (UMLS CUI [1])
clinical relapse
Item
have clinical relapse 30 days prior to randomisation
boolean
C0856120 (UMLS CUI [1])

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