Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Einschlusskriterien
Description

Einschlusskriterien

Age
Description

Age

Data type

boolean

Relapsing multiple sclerosis
Description

Relapsing multiple sclerosis

Data type

boolean

Neurological state
Description

Neurological state

Data type

boolean

EDSS
Description

EDSS

Data type

boolean

No pregnancy, no breast feeding
Description

No pregnancy, no breast feeding

Data type

boolean

Ausschlusskriterien
Description

Ausschlusskriterien

Progressive MS
Description

Progressive MS

Data type

boolean

Prior use of any interferon or glatiramer acetate
Description

Prior use of any interferon or glatiramer acetate

Data type

boolean

Steroid treatment
Description

Steroid treatment

Data type

boolean

Psychiatric disorder
Description

Psychiatric disorder

Data type

boolean

Leukopenia
Description

Leukopenia

Data type

boolean

Liver disease
Description

Liver disease

Data type

boolean

Prior cytokine or anti-cytokine therapy
Description

Prior cytokine or anti-cytokine therapy

Data type

boolean

Prior use of immunomodulatory or immunosuppressive therapy
Description

Prior use of immunomodulatory or immunosuppressive therapy

Data type

boolean

Prior use of cladribine or have received total lymphoid irradiation
Description

Prior use of cladribine or have received total lymphoid irradiation

Data type

boolean

Allergy or hypersensitivity
Description

Allergy or hypersensitivity

Data type

boolean

Investigational drugs
Description

Investigational drugs

Data type

boolean

Systemic disease
Description

Systemic disease

Data type

boolean

Plasma exchange
Description

Plasma exchange

Data type

boolean

Medizinische Konzepte
Description

Medizinische Konzepte

Age
Description

Age

Data type

string

Alias
UMLS CUI
C0001779
SNOMED CT 2010_0731
102518004
Diagnosis
Description

Diagnosis

Data type

string

Alias
UMLS CUI
C0011900
SNOMED CT 2010_0731
439401001
Relapsing multiple sclerosis
Description

Relapsing multiple sclerosis

Data type

string

Alias
UMLS CUI
C0751967
MedDRA Version 13.1
10063399
SNOMED CT 2010_0731
426373005
EDSS
Description

EDSS

Data type

string

Alias
UMLS CUI
C0451246
SNOMED CT 2010_0731
273554001
pregnant
Description

pregnant

Data type

string

Alias
UMLS CUI
C0549206
MedDRA 13.1
10036586
Breast feeding
Description

Breast feeding

Data type

string

Alias
UMLS CUI
C0006147
MedDRA 13.1
10006247
Serum HCG
Description

Serum HCG

Data type

string

Alias
UMLS CUI
C2348195
LOINC
2118-8
MedDRA 13.1
10036572
Progressive multiple sclerosis
Description

Progressive multiple sclerosis

Data type

string

Alias
UMLS CUI
C0393665
MedDRA Version 13.1
10053395
Pharmaceutical Preparations
Description

Pharmaceutical Preparations

Data type

string

Alias
UMLS CUI
C0013227
Psychiatric disorder
Description

Psychiatric disorder

Data type

string

Alias
UMLS CUI
C0004936
MedDRA Version 13.1
10037175
SNOMED CT 2010_0731
74732009
CTCAE Version 4.03
E13867
WBC
Description

WBC

Data type

string

Alias
SNOMED CT 2010_0731
767002
LOINC
6690-2
AST
Description

AST

Data type

string

Alias
SNOMED CT 2010_0731
26091008
UMLS CUI
C0004002
MedDRA Version 13.1
10003543
LOINC
1920-8
ALT
Description

ALT

Data type

string

Alias
SNOMED CT 2010_0731
56935002
UMLS CUI
C0001899
MedDRA Version 13.1
10001844
LOINC
1742-6
Radiotherapy
Description

Radiotherapy

Data type

string

Alias
UMLS CUI
C1522449
SNOMED CT 2010_0731
302505005
Allergic reaction, due to correct medicinal substance properly administered
Description

Allergic reaction, due to correct medicinal substance properly administered

Data type

string

Alias
UMLS CUI
C0274302
SNOMED CT 2010_0731
57302007
Therapeutic procedure
Description

Therapeutic procedure

Data type

string

Alias
UMLS CUI
C0087111

Similar models

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Einschlusskriterien
Age
Item
boolean
Relapsing multiple sclerosis
Item
boolean
Neurological state
Item
boolean
EDSS
Item
boolean
No pregnancy, no breast feeding
Item
boolean
Item Group
Ausschlusskriterien
Progressive MS
Item
boolean
Prior use of any interferon or glatiramer acetate
Item
boolean
Steroid treatment
Item
boolean
Psychiatric disorder
Item
boolean
Leukopenia
Item
boolean
Liver disease
Item
boolean
Prior cytokine or anti-cytokine therapy
Item
boolean
Prior use of immunomodulatory or immunosuppressive therapy
Item
boolean
Prior use of cladribine or have received total lymphoid irradiation
Item
boolean
Allergy or hypersensitivity
Item
boolean
Investigational drugs
Item
boolean
Systemic disease
Item
boolean
Plasma exchange
Item
boolean
Item Group
Medizinische Konzepte
Age
Item
string
C0001779 (UMLS CUI)
102518004 (SNOMED CT 2010_0731)
Diagnosis
Item
string
C0011900 (UMLS CUI)
439401001 (SNOMED CT 2010_0731)
Relapsing multiple sclerosis
Item
string
C0751967 (UMLS CUI)
10063399 (MedDRA Version 13.1)
426373005 (SNOMED CT 2010_0731)
EDSS
Item
string
C0451246 (UMLS CUI)
273554001 (SNOMED CT 2010_0731)
pregnant
Item
string
C0549206 (UMLS CUI)
10036586 (MedDRA 13.1)
Breast feeding
Item
string
C0006147 (UMLS CUI)
10006247 (MedDRA 13.1)
Serum HCG
Item
string
C2348195 (UMLS CUI)
2118-8 (LOINC)
10036572 (MedDRA 13.1)
Progressive multiple sclerosis
Item
string
C0393665 (UMLS CUI)
10053395 (MedDRA Version 13.1)
Pharmaceutical Preparations
Item
string
C0013227 (UMLS CUI)
Psychiatric disorder
Item
string
C0004936 (UMLS CUI)
10037175 (MedDRA Version 13.1)
74732009 (SNOMED CT 2010_0731)
E13867 (CTCAE Version 4.03)
WBC
Item
string
767002 (SNOMED CT 2010_0731)
6690-2 (LOINC)
AST
Item
string
26091008 (SNOMED CT 2010_0731)
C0004002 (UMLS CUI)
10003543 (MedDRA Version 13.1)
1920-8 (LOINC)
ALT
Item
string
56935002 (SNOMED CT 2010_0731)
C0001899 (UMLS CUI)
10001844 (MedDRA Version 13.1)
1742-6 (LOINC)
Radiotherapy
Item
string
C1522449 (UMLS CUI)
302505005 (SNOMED CT 2010_0731)
Allergic reaction, due to correct medicinal substance properly administered
Item
string
C0274302 (UMLS CUI)
57302007 (SNOMED CT 2010_0731)
Therapeutic procedure
Item
string
C0087111 (UMLS CUI)