ID

30954

Beschreibung

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

Stichworte

  1. 07.07.18 07.07.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

7. Juli 2018

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT01079975

Eligibility Multiple Sclerosis NCT01079975

Inclusion Criteria
Beschreibung

Inclusion Criteria

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

Age

Datentyp

boolean

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

Multiple Sclerosis

Datentyp

boolean

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

Multiple Sclerosis Type Any

Datentyp

boolean

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

Informed Consent

Datentyp

boolean

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

Protocol Compliance

Datentyp

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Beschreibung

Exclusion Criteria

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

Depressive disorder

Datentyp

boolean

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

Antidepressive Agents

Datentyp

boolean

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

Moderate cognitive impairment | Severe cognitive impairment

Datentyp

boolean

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

Mental disorders

Datentyp

boolean

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

Therapy, investigational

Datentyp

boolean

Alias
UMLS CUI [1]
C0949266

Ähnliche Modelle

Eligibility Multiple Sclerosis NCT01079975

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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