Informatie:
Fout:
ID
13969
Beschrijving
Fatigue Treatment Using Provigil; ODM derived from: https://clinicaltrials.gov/show/NCT00220506
Link
https://clinicaltrials.gov/show/NCT00220506
Trefwoorden
Versies (1)
- 20-03-16 20-03-16 -
Geüploaded op
20 maart 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility All Multiple Sclerosis Patients NCT00220506
Eligibility All Multiple Sclerosis Patients NCT00220506
- StudyEvent: Eligibility
Similar models
Eligibility All Multiple Sclerosis Patients NCT00220506
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
C0700589 (UMLS CUI [1,2])
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])
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])
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])