Eligibility All Multiple Sclerosis Patients NCT00220506

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
Multiple Sclerosis
Description

MS

Data type

text

Alias
UMLS CUI [1]
C0026769
EDSS score from 0 to 5.5, inclusive
Description

EDSS

Data type

boolean

Alias
UMLS CUI [1]
C0451246
positive fatigue impact scale 40 points or more.
Description

fatigue impact scale

Data type

boolean

Alias
UMLS CUI [1]
C2733557
Age
Description

Age

Data type

text

Measurement units
  • years
Alias
UMLS CUI [1]
C0001779
years
Patient is willing and able to comply to study protocol
Description

Compliance behavior

Data type

boolean

Alias
UMLS CUI [1]
C1321605
Written informed consent
Description

Written informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Women of childbearing potential
Description

Childbearing potential

Data type

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
Patient is willing and able to comply to study protocol
Description

Compliance behavior

Data type

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
Recurrent Disease
Description

Relapse

Data type

text

Alias
UMLS CUI [1]
C0277556
systemic steroid therapy within 30 days
Description

systemic steroid therapy

Data type

boolean

Alias
UMLS CUI [1]
C4039704
known hypersensitivity or intolerance, to provigil or related substances or to any component of the formulation.
Description

hypersensitivity to provigil

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0722882
patients, who have a risk professional with symptomatic sleep apnea
Description

sleep apnea

Data type

boolean

Alias
UMLS CUI [1]
C0037315
known to suffer from narcolepsy or another significant sleep disorder.
Description

Narcolepsy

Data type

boolean

Alias
UMLS CUI [1]
C0027404
Subject Participation Status in Clinical Study
Description

Study Subject Participation Status

Data type

text

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility All Multiple Sclerosis Patients NCT00220506

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
MS
Item
Multiple Sclerosis
text
C0026769 (UMLS CUI [1])
EDSS
Item
EDSS score from 0 to 5.5, inclusive
boolean
C0451246 (UMLS CUI [1])
fatigue impact scale
Item
positive fatigue impact scale 40 points or more.
boolean
C2733557 (UMLS CUI [1])
Age
Item
Age
text
C0001779 (UMLS CUI [1])
Compliance behavior
Item
Patient is willing and able to comply to study protocol
boolean
C1321605 (UMLS CUI [1])
Written informed consent
Item
Written informed consent
boolean
C0021430 (UMLS CUI [1])
Childbearing potential
Item
Women of childbearing potential
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Compliance behavior
Item
Patient is willing and able to comply to study protocol
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
Relapse
Item
Recurrent Disease
text
C0277556 (UMLS CUI [1])
systemic steroid therapy
Item
systemic steroid therapy within 30 days
boolean
C4039704 (UMLS CUI [1])
hypersensitivity to provigil
Item
known hypersensitivity or intolerance, to provigil or related substances or to any component of the formulation.
boolean
C0020517 (UMLS CUI [1,1])
C0722882 (UMLS CUI [1,2])
sleep apnea
Item
patients, who have a risk professional with symptomatic sleep apnea
boolean
C0037315 (UMLS CUI [1])
Narcolepsy
Item
known to suffer from narcolepsy or another significant sleep disorder.
boolean
C0027404 (UMLS CUI [1])
Study Subject Participation Status
Item
Subject Participation Status in Clinical Study
text
C2348568 (UMLS CUI [1])