Eligibility Relapsing-remitting Multiple Sclerosis NCT01006265

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult males and females
Description

Adult

Data type

boolean

Alias
UMLS CUI [1]
C0001675
diagnosis of rrms as defined by the revised (2005) mcdonald diagnostic criteria for multiple sclerosis (ms).
Description

Multiple Sclerosis, Relapsing-Remitting

Data type

boolean

Alias
UMLS CUI [1]
C0751967
signed inform consent prior to initiation of any study-mandated procedure.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
a diagnosis of ms categorized as primary progressive or secondary progressive or progressive relapsing.
Description

Multiple Sclerosis, Primary Progressive | Multiple Sclerosis, Secondary Progressive | Multiple Sclerosis, Progressive Relapsing

Data type

boolean

Alias
UMLS CUI [1]
C0751964
UMLS CUI [2]
C0751965
UMLS CUI [3]
C0393666
patients currently treated for an autoimmune disorder other than ms.
Description

Therapeutic procedure Autoimmune Disease | Exception Multiple Sclerosis

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0004364
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0026769
contraindications for mri.
Description

Medical contraindication MRI

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
ongoing bacterial, viral, or fungal infection.
Description

Bacterial Infection | Viral infection | Mycoses

Data type

boolean

Alias
UMLS CUI [1]
C0004623
UMLS CUI [2]
C0042769
UMLS CUI [3]
C0026946
history or presence of malignancy.
Description

Malignant Neoplasms

Data type

boolean

Alias
UMLS CUI [1]
C0006826
additional inclusion and exclusion criteria apply with respect to medical conditions and concomitant treatments which could affect patients' risk from participating in the study.
Description

Eligibility Criteria Additional | Medical condition Study Subject Participation Status At risk | Therapeutic procedure Study Subject Participation Status At risk

Data type

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C1524062
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C1444641
UMLS CUI [3,1]
C0087111
UMLS CUI [3,2]
C2348568
UMLS CUI [3,3]
C1444641

Similar models

Eligibility Relapsing-remitting Multiple Sclerosis NCT01006265

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Adult
Item
adult males and females
boolean
C0001675 (UMLS CUI [1])
Multiple Sclerosis, Relapsing-Remitting
Item
diagnosis of rrms as defined by the revised (2005) mcdonald diagnostic criteria for multiple sclerosis (ms).
boolean
C0751967 (UMLS CUI [1])
Informed Consent
Item
signed inform consent prior to initiation of any study-mandated procedure.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Multiple Sclerosis, Primary Progressive | Multiple Sclerosis, Secondary Progressive | Multiple Sclerosis, Progressive Relapsing
Item
a diagnosis of ms categorized as primary progressive or secondary progressive or progressive relapsing.
boolean
C0751964 (UMLS CUI [1])
C0751965 (UMLS CUI [2])
C0393666 (UMLS CUI [3])
Therapeutic procedure Autoimmune Disease | Exception Multiple Sclerosis
Item
patients currently treated for an autoimmune disorder other than ms.
boolean
C0087111 (UMLS CUI [1,1])
C0004364 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0026769 (UMLS CUI [2,2])
Medical contraindication MRI
Item
contraindications for mri.
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
Bacterial Infection | Viral infection | Mycoses
Item
ongoing bacterial, viral, or fungal infection.
boolean
C0004623 (UMLS CUI [1])
C0042769 (UMLS CUI [2])
C0026946 (UMLS CUI [3])
Malignant Neoplasms
Item
history or presence of malignancy.
boolean
C0006826 (UMLS CUI [1])
Eligibility Criteria Additional | Medical condition Study Subject Participation Status At risk | Therapeutic procedure Study Subject Participation Status At risk
Item
additional inclusion and exclusion criteria apply with respect to medical conditions and concomitant treatments which could affect patients' risk from participating in the study.
boolean
C1516637 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
C3843040 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C1444641 (UMLS CUI [2,3])
C0087111 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C1444641 (UMLS CUI [3,3])