ID

22920

Descrizione

Clinical Trial Comparing Treatment of Relapsing-Remitting Multiple Sclerosis (RR-MS) With Two Doses of Glatiramer Acetate (GA).; ODM derived from: https://clinicaltrials.gov/show/NCT00337779

collegamento

https://clinicaltrials.gov/show/NCT00337779

Keywords

versioni (1)
  1. 16/06/17 16/06/17 -
Caricato su

16 giugno 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Relapsing Remitting Multiple Sclerosis NCT00337779

Inglese

Eligibility Relapsing Remitting Multiple Sclerosis NCT00337779

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. diagnosis of confirmed and documented ms defined by the revised mcdonald criteria.
Descrizione

Multiple Sclerosis

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0026769
2. subjects must be of the relapsing-remitting (r-r) type.
Descrizione

Multiple Sclerosis, Relapsing-Remitting

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0751967
3. subject has experienced prior to screening at least one documented relapse in 12 months or at least 2 documented relapses in the 24 months or one documented relapse between 12 - 24 months with at least 1 documented t1-gd enhancing lesion in the mri performed 12 months prior screening.
Descrizione

Relapse Quantity | Gadolinium-Enhancing Lesion Quantity Magnetic Resonance Imaging

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0035020
UMLS CUI [1,2]
C1265611
UMLS CUI [2,1]
C1333400
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0024485
4. disease duration for at least 6 months.
Descrizione

disease length

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0872146
5. ambulatory with converted kurtzke edss score of 0 - 5.
Descrizione

Ambulatory Kurtzke multiple sclerosis rating scale

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0439841
UMLS CUI [1,2]
C0451246
6. relapse free and stable neurological condition at least for 30 days prior screening.
Descrizione

Condition Neurologic Stable | Relapse Free of

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0205494
UMLS CUI [1,3]
C0205360
UMLS CUI [2,1]
C0035020
UMLS CUI [2,2]
C0332296
7. age - 18-55 (inclusive)
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. previous use of copaxone (glatiramer acetate)
Descrizione

Copaxone | glatiramer acetate

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0528175
UMLS CUI [2]
C0289884
2. treatment with corticosteroids within 30 days prior screening or between screening and baseline.
Descrizione

Adrenal Cortex Hormones

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001617
3. chronic corticosteroids treatment - more than 30 consecutive days.
Descrizione

Adrenal Cortex Hormones chronic

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C0205191
4. subject with any clinically significant or unstable medical condition.
Descrizione

Medical condition Clinical Significance | Medical condition Unstable

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C2826293
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C0443343
5. subjects participating in any other clinical trial (within 12 weeks prior to screening and thereafter).
Descrizione

Study Subject Participation Status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568
6. known history of sensitivity to gadolinium and inability to successfully undergo mri scanning.
Descrizione

Hypersensitivity Gadolinium | Magnetic Resonance Imaging Receive Unable

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0016911
UMLS CUI [2,1]
C0024485
UMLS CUI [2,2]
C1514756
UMLS CUI [2,3]
C1299582
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Similar models

Eligibility Relapsing Remitting Multiple Sclerosis NCT00337779

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Multiple Sclerosis
Item
1. diagnosis of confirmed and documented ms defined by the revised mcdonald criteria.
boolean
C0026769 (UMLS CUI [1])
Multiple Sclerosis, Relapsing-Remitting
Item
2. subjects must be of the relapsing-remitting (r-r) type.
boolean
C0751967 (UMLS CUI [1])
Relapse Quantity | Gadolinium-Enhancing Lesion Quantity Magnetic Resonance Imaging
Item
3. subject has experienced prior to screening at least one documented relapse in 12 months or at least 2 documented relapses in the 24 months or one documented relapse between 12 - 24 months with at least 1 documented t1-gd enhancing lesion in the mri performed 12 months prior screening.
boolean
C0035020 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1333400 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0024485 (UMLS CUI [2,3])
disease length
Item
4. disease duration for at least 6 months.
boolean
C0872146 (UMLS CUI [1])
Ambulatory Kurtzke multiple sclerosis rating scale
Item
5. ambulatory with converted kurtzke edss score of 0 - 5.
boolean
C0439841 (UMLS CUI [1,1])
C0451246 (UMLS CUI [1,2])
Condition Neurologic Stable | Relapse Free of
Item
6. relapse free and stable neurological condition at least for 30 days prior screening.
boolean
C0348080 (UMLS CUI [1,1])
C0205494 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0035020 (UMLS CUI [2,1])
C0332296 (UMLS CUI [2,2])
Age
Item
7. age - 18-55 (inclusive)
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Copaxone | glatiramer acetate
Item
1. previous use of copaxone (glatiramer acetate)
boolean
C0528175 (UMLS CUI [1])
C0289884 (UMLS CUI [2])
Adrenal Cortex Hormones
Item
2. treatment with corticosteroids within 30 days prior screening or between screening and baseline.
boolean
C0001617 (UMLS CUI [1])
Adrenal Cortex Hormones chronic
Item
3. chronic corticosteroids treatment - more than 30 consecutive days.
boolean
C0001617 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
Medical condition Clinical Significance | Medical condition Unstable
Item
4. subject with any clinically significant or unstable medical condition.
boolean
C3843040 (UMLS CUI [1,1])
C2826293 (UMLS CUI [1,2])
C3843040 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
Study Subject Participation Status
Item
5. subjects participating in any other clinical trial (within 12 weeks prior to screening and thereafter).
boolean
C2348568 (UMLS CUI [1])
Hypersensitivity Gadolinium | Magnetic Resonance Imaging Receive Unable
Item
6. known history of sensitivity to gadolinium and inability to successfully undergo mri scanning.
boolean
C0020517 (UMLS CUI [1,1])
C0016911 (UMLS CUI [1,2])
C0024485 (UMLS CUI [2,1])
C1514756 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
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