ID

13969

Descripción

Fatigue Treatment Using Provigil; ODM derived from: https://clinicaltrials.gov/show/NCT00220506

Link

https://clinicaltrials.gov/show/NCT00220506

Palabras clave

  1. 20/3/16 20/3/16 -
Subido en

20 de marzo de 2016

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility All Multiple Sclerosis Patients NCT00220506

Eligibility All Multiple Sclerosis Patients NCT00220506

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
Multiple Sclerosis
Descripción

MS

Tipo de datos

text

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

EDSS

Tipo de datos

boolean

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

fatigue impact scale

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2733557
Age
Descripción

Age

Tipo de datos

text

Unidades de medida
  • years
Alias
UMLS CUI [1]
C0001779
years
Patient is willing and able to comply to study protocol
Descripción

Compliance behavior

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1321605
Written informed consent
Descripción

Written informed consent

Tipo de datos

boolean

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

Childbearing potential

Tipo de datos

boolean

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

Exclusion Criteria

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

Compliance behavior

Tipo de datos

boolean

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

Relapse

Tipo de datos

text

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

systemic steroid therapy

Tipo de datos

boolean

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

hypersensitivity to provigil

Tipo de datos

boolean

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

sleep apnea

Tipo de datos

boolean

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

Narcolepsy

Tipo de datos

boolean

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

Study Subject Participation Status

Tipo de datos

text

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility All Multiple Sclerosis Patients NCT00220506

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])

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