ID

13767

Description

BRAVE-DREAMS (BRAin VEnous DRainage Exploited Against Multiple Sclerosis); ODM derived from: https://clinicaltrials.gov/show/NCT01371760

Lien

https://clinicaltrials.gov/show/NCT01371760

Mots-clés

  1. 06/03/2016 06/03/2016 -
Téléchargé le

6 mars 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT01371760

Eligibility Multiple Sclerosis NCT01371760

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients affected by ccsvi associated with ms
Description

Chronic venous insufficiency Cerebrospinal angiopathy; Multiple Sclerosis

Type de données

boolean

Alias
UMLS CUI [1,1]
C1306557
UMLS CUI [1,2]
C0276094
UMLS CUI [2]
C0026769
relapsing-remitting and\or secondary progressive
Description

relapse; Multiple Sclerosis, Secondary Progressive

Type de données

boolean

Alias
UMLS CUI [1]
C0277556
UMLS CUI [2]
C0751965
18-65 years old
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
edss 2-5
Description

Expanded Disability Status Scale

Type de données

boolean

Alias
UMLS CUI [1]
C0451246
disease duration < 10y
Description

duration disease

Type de données

boolean

Alias
UMLS CUI [1]
C0872146
no relapse in the 30 days preceding the procedure
Description

relapse

Type de données

boolean

Alias
UMLS CUI [1]
C0277556
clinical stability in the last 6 months with disease mod. treatments
Description

Stable Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0677946
patients under the best available therapy
Description

therapy multiple sclerosis

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0026769
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients previously treated for ccsvi or inserted in other clinical trials in the last 3 months
Description

Study Subject Participation Status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
under treatment with natalizumab
Description

therapy natalizumab

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C1172734
pregnant or refusing to adopt contraception
Description

contraception status; Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0420837
UMLS CUI [2]
C0032961
presence of significant comorbidities
Description

comorbidity

Type de données

boolean

Alias
UMLS CUI [1]
C0009488
alcool-drug abuse
Description

Substance Use Disorder

Type de données

boolean

Alias
UMLS CUI [1]
C0038586
thrombophilia
Description

thrombophilia

Type de données

boolean

Alias
UMLS CUI [1]
C0398623
contraindication to mr
Description

contraindication Magnetic Resonance

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0917874

Similar models

Eligibility Multiple Sclerosis NCT01371760

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Chronic venous insufficiency Cerebrospinal angiopathy; Multiple Sclerosis
Item
patients affected by ccsvi associated with ms
boolean
C1306557 (UMLS CUI [1,1])
C0276094 (UMLS CUI [1,2])
C0026769 (UMLS CUI [2])
relapse; Multiple Sclerosis, Secondary Progressive
Item
relapsing-remitting and\or secondary progressive
boolean
C0277556 (UMLS CUI [1])
C0751965 (UMLS CUI [2])
age
Item
18-65 years old
boolean
C0001779 (UMLS CUI [1])
Expanded Disability Status Scale
Item
edss 2-5
boolean
C0451246 (UMLS CUI [1])
duration disease
Item
disease duration < 10y
boolean
C0872146 (UMLS CUI [1])
relapse
Item
no relapse in the 30 days preceding the procedure
boolean
C0277556 (UMLS CUI [1])
Stable Disease
Item
clinical stability in the last 6 months with disease mod. treatments
boolean
C0677946 (UMLS CUI [1])
therapy multiple sclerosis
Item
patients under the best available therapy
boolean
C0087111 (UMLS CUI [1,1])
C0026769 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Study Subject Participation Status
Item
patients previously treated for ccsvi or inserted in other clinical trials in the last 3 months
boolean
C2348568 (UMLS CUI [1])
therapy natalizumab
Item
under treatment with natalizumab
boolean
C0087111 (UMLS CUI [1,1])
C1172734 (UMLS CUI [1,2])
contraception status; Pregnancy
Item
pregnant or refusing to adopt contraception
boolean
C0420837 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
comorbidity
Item
presence of significant comorbidities
boolean
C0009488 (UMLS CUI [1])
Substance Use Disorder
Item
alcool-drug abuse
boolean
C0038586 (UMLS CUI [1])
thrombophilia
Item
thrombophilia
boolean
C0398623 (UMLS CUI [1])
contraindication Magnetic Resonance
Item
contraindication to mr
boolean
C1301624 (UMLS CUI [1,1])
C0917874 (UMLS CUI [1,2])

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