ID

30954

Beschrijving

To Identify and Evaluate the Predictive Factors for Depression in Patients Diagnosed With Multiple Sclerosis; ODM derived from: https://clinicaltrials.gov/show/NCT01079975

Link

https://clinicaltrials.gov/show/NCT01079975

Trefwoorden

  1. 07-07-18 07-07-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

7 juli 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT01079975

Eligibility Multiple Sclerosis NCT01079975

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects aged between 18 65 years of both sexes
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
subjects with established ms diagnosis according to the revised mc donald criteria -
Beschrijving

Multiple Sclerosis

Datatype

boolean

Alias
UMLS CUI [1]
C0026769
2005 in any of its clinical forms
Beschrijving

Multiple Sclerosis Type Any

Datatype

boolean

Alias
UMLS CUI [1,1]
C0026769
UMLS CUI [1,2]
C0332307
UMLS CUI [1,3]
C1552551
subjects with signed informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
subjects wiling to follow the study procedure
Beschrijving

Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects with diagnosis of depression at the moment of the initial evaluation
Beschrijving

Depressive disorder

Datatype

boolean

Alias
UMLS CUI [1]
C0011581
subjects receiving antidepressant drugs at the moment of the initial evaluation
Beschrijving

Antidepressive Agents

Datatype

boolean

Alias
UMLS CUI [1]
C0003289
subjects with moderate or severe cognitive impairment
Beschrijving

Moderate cognitive impairment | Severe cognitive impairment

Datatype

boolean

Alias
UMLS CUI [1]
C3839816
UMLS CUI [2]
C3554639
antecedents of any other psychiatric disease
Beschrijving

Mental disorders

Datatype

boolean

Alias
UMLS CUI [1]
C0004936
subjects that were receiving or have received any experimental treatment during the 6 months before the inclusion
Beschrijving

Therapy, investigational

Datatype

boolean

Alias
UMLS CUI [1]
C0949266

Similar models

Eligibility Multiple Sclerosis NCT01079975

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
subjects aged between 18 65 years of both sexes
boolean
C0001779 (UMLS CUI [1])
Multiple Sclerosis
Item
subjects with established ms diagnosis according to the revised mc donald criteria -
boolean
C0026769 (UMLS CUI [1])
Multiple Sclerosis Type Any
Item
2005 in any of its clinical forms
boolean
C0026769 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C1552551 (UMLS CUI [1,3])
Informed Consent
Item
subjects with signed informed consent
boolean
C0021430 (UMLS CUI [1])
Protocol Compliance
Item
subjects wiling to follow the study procedure
boolean
C0525058 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Depressive disorder
Item
subjects with diagnosis of depression at the moment of the initial evaluation
boolean
C0011581 (UMLS CUI [1])
Antidepressive Agents
Item
subjects receiving antidepressant drugs at the moment of the initial evaluation
boolean
C0003289 (UMLS CUI [1])
Moderate cognitive impairment | Severe cognitive impairment
Item
subjects with moderate or severe cognitive impairment
boolean
C3839816 (UMLS CUI [1])
C3554639 (UMLS CUI [2])
Mental disorders
Item
antecedents of any other psychiatric disease
boolean
C0004936 (UMLS CUI [1])
Therapy, investigational
Item
subjects that were receiving or have received any experimental treatment during the 6 months before the inclusion
boolean
C0949266 (UMLS CUI [1])

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