ID

15612

Description

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

Lien

https://clinicaltrials.gov/show/NCT00151801

Mots-clés

  1. 05/06/2016 05/06/2016 -
Téléchargé le

5 juin 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT00151801

Eligibility Multiple Sclerosis NCT00151801

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female patients
Description

female patients

Type de données

boolean

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

relapsing-remitting ms

Type de données

boolean

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

age

Type de données

boolean

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

edss

Type de données

boolean

Alias
UMLS CUI [1]
C0451246
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of migraine or thromboembolic events
Description

migraine or thromboembolic events

Type de données

boolean

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

reproductive system disorders

Type de données

boolean

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

pregnancy

Type de données

boolean

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

estroprogestins

Type de données

boolean

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

immunosuppressive drugs

Type de données

boolean

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

immunomodulating drugs

Type de données

boolean

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

corticosteroids

Type de données

boolean

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

clinical relapse

Type de données

boolean

Alias
UMLS CUI [1]
C0856120

Similar models

Eligibility Multiple Sclerosis NCT00151801

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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