ID

14655

Beschrijving

Evaluation of a New Therapeutic Strategy in Early and Active Relapsing-Remitting Multiple Sclerosis; ODM derived from: https://clinicaltrials.gov/show/NCT00219908

Link

https://clinicaltrials.gov/show/NCT00219908

Trefwoorden

  1. 25-04-16 25-04-16 -
Geüploaded op

25 april 2016

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Relapsing-Remitting Multiple Sclerosis NCT00219908

Eligibility Relapsing-Remitting Multiple Sclerosis NCT00219908

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
age : 18-45 years,
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
clinical disease satisfying the poser criteria (amdmt n°4)
Beschrijving

Clinical disease

Datatype

boolean

Alias
UMLS CUI [1]
C0012634
relapsing-remitting disease (amdmt n°4)
Beschrijving

Relapsing-Remitting Multiple Sclerosis

Datatype

boolean

Alias
UMLS CUI [1]
C0751967
at least 2 exacerbations within the preceding 12 months, having left sequelae,
Beschrijving

MS exacerbation

Datatype

boolean

Alias
UMLS CUI [1]
C0581392
mri activity at inclusion expressed by at least one gadolinium-enhanced lesion (cranial mri with 0.1mmol/kg gadolinium),
Beschrijving

MRI with gadolinium

Datatype

boolean

Alias
UMLS CUI [1,1]
C0024485
UMLS CUI [1,2]
C0016911
a significant disability at inclusion: edss score between 2.5 and 5.5 (amdt n° 4)
Beschrijving

EDSS score

Datatype

boolean

Alias
UMLS CUI [1]
C0451246
written informed consent
Beschrijving

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy and breast-feeding
Beschrijving

Gynaecological status

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
use of an insufficiency effective contraceptive method,
Beschrijving

Contraception

Datatype

boolean

Alias
UMLS CUI [1]
C0700589
general immunosuppressive therapy using cyclophosphamide, mitoxantrone,or total lymphoid irradiation
Beschrijving

iImunosuppressive therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0021079
treatment with azathioprine during the 3 months preceding the study
Beschrijving

Azathioprine

Datatype

boolean

Alias
UMLS CUI [1]
C0004482
clinical relapse or intensive corticosteroid treatment within the 30 days preceding inclusion,
Beschrijving

Relapse and corticosteroid treatment

Datatype

boolean

Alias
UMLS CUI [1]
C0277556
UMLS CUI [2]
C0149783
associated disease (psychiatric disorder, depressive statenot controlled by appropriate drug therapy, history of heart disease at inclusion examination
Beschrijving

Comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0009488

Similar models

Eligibility Relapsing-Remitting Multiple Sclerosis NCT00219908

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age : 18-45 years,
boolean
C0001779 (UMLS CUI [1])
Clinical disease
Item
clinical disease satisfying the poser criteria (amdmt n°4)
boolean
C0012634 (UMLS CUI [1])
Relapsing-Remitting Multiple Sclerosis
Item
relapsing-remitting disease (amdmt n°4)
boolean
C0751967 (UMLS CUI [1])
MS exacerbation
Item
at least 2 exacerbations within the preceding 12 months, having left sequelae,
boolean
C0581392 (UMLS CUI [1])
MRI with gadolinium
Item
mri activity at inclusion expressed by at least one gadolinium-enhanced lesion (cranial mri with 0.1mmol/kg gadolinium),
boolean
C0024485 (UMLS CUI [1,1])
C0016911 (UMLS CUI [1,2])
EDSS score
Item
a significant disability at inclusion: edss score between 2.5 and 5.5 (amdt n° 4)
boolean
C0451246 (UMLS CUI [1])
Informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Gynaecological status
Item
pregnancy and breast-feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Contraception
Item
use of an insufficiency effective contraceptive method,
boolean
C0700589 (UMLS CUI [1])
iImunosuppressive therapy
Item
general immunosuppressive therapy using cyclophosphamide, mitoxantrone,or total lymphoid irradiation
boolean
C0021079 (UMLS CUI [1])
Azathioprine
Item
treatment with azathioprine during the 3 months preceding the study
boolean
C0004482 (UMLS CUI [1])
Relapse and corticosteroid treatment
Item
clinical relapse or intensive corticosteroid treatment within the 30 days preceding inclusion,
boolean
C0277556 (UMLS CUI [1])
C0149783 (UMLS CUI [2])
Comorbidity
Item
associated disease (psychiatric disorder, depressive statenot controlled by appropriate drug therapy, history of heart disease at inclusion examination
boolean
C0009488 (UMLS CUI [1])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial