Eligibility Multiple Sclerosis NCT02377323

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with cis or definite ms (rrms or spms);
Description

Clinically isolated syndrome | Multiple Sclerosis | Multiple Sclerosis, Relapsing-Remitting | Multiple Sclerosis, Secondary Progressive

Data type

boolean

Alias
UMLS CUI [1]
C2921627
UMLS CUI [2]
C0026769
UMLS CUI [3]
C0751967
UMLS CUI [4]
C0751965
patients seen at our clinic within the last 2 years;
Description

Clinic Visit

Data type

boolean

Alias
UMLS CUI [1]
C0008952
patients untreated, or treated with either low dose or high dose rebif for at least two years;
Description

Patients Untreated | Rebif Low dose | Rebif High dose

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0332155
UMLS CUI [2,1]
C0752980
UMLS CUI [2,2]
C0445550
UMLS CUI [3,1]
C0752980
UMLS CUI [3,2]
C0444956
patients between 18 to 60 years old at time of treatment initiation;
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
edss ≤ 5.5 at treatment initiation;
Description

EDSS

Data type

boolean

Alias
UMLS CUI [1]
C0451246
patients able to read and write in french.
Description

Able to read French language | Able to write French language

Data type

boolean

Alias
UMLS CUI [1,1]
C0586740
UMLS CUI [1,2]
C0376246
UMLS CUI [2,1]
C0584993
UMLS CUI [2,2]
C0376246
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients diagnosed with primary progressive ms;
Description

Multiple Sclerosis, Primary Progressive

Data type

boolean

Alias
UMLS CUI [1]
C0751964
patients treated with other dmd, other than rebif;
Description

Disease Modification Pharmaceutical Preparations | Exception Rebif

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C3840684
UMLS CUI [1,3]
C0013227
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0752980
co-existence of other diseases that could influence outcomes.
Description

Comorbidity Influence Research results

Data type

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C4054723
UMLS CUI [1,3]
C0683954

Similar models

Eligibility Multiple Sclerosis NCT02377323

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Clinically isolated syndrome | Multiple Sclerosis | Multiple Sclerosis, Relapsing-Remitting | Multiple Sclerosis, Secondary Progressive
Item
patients with cis or definite ms (rrms or spms);
boolean
C2921627 (UMLS CUI [1])
C0026769 (UMLS CUI [2])
C0751967 (UMLS CUI [3])
C0751965 (UMLS CUI [4])
Clinic Visit
Item
patients seen at our clinic within the last 2 years;
boolean
C0008952 (UMLS CUI [1])
Patients Untreated | Rebif Low dose | Rebif High dose
Item
patients untreated, or treated with either low dose or high dose rebif for at least two years;
boolean
C0030705 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0752980 (UMLS CUI [2,1])
C0445550 (UMLS CUI [2,2])
C0752980 (UMLS CUI [3,1])
C0444956 (UMLS CUI [3,2])
Age
Item
patients between 18 to 60 years old at time of treatment initiation;
boolean
C0001779 (UMLS CUI [1])
EDSS
Item
edss ≤ 5.5 at treatment initiation;
boolean
C0451246 (UMLS CUI [1])
Able to read French language | Able to write French language
Item
patients able to read and write in french.
boolean
C0586740 (UMLS CUI [1,1])
C0376246 (UMLS CUI [1,2])
C0584993 (UMLS CUI [2,1])
C0376246 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Multiple Sclerosis, Primary Progressive
Item
patients diagnosed with primary progressive ms;
boolean
C0751964 (UMLS CUI [1])
Disease Modification Pharmaceutical Preparations | Exception Rebif
Item
patients treated with other dmd, other than rebif;
boolean
C0012634 (UMLS CUI [1,1])
C3840684 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C0752980 (UMLS CUI [2,2])
Comorbidity Influence Research results
Item
co-existence of other diseases that could influence outcomes.
boolean
C0009488 (UMLS CUI [1,1])
C4054723 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])