ID

34454

Beschrijving

Emotional and Cognitive Subthalamic Nucleus in Deep Brain Stimulation Treated Parkinson Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01590056

Link

https://clinicaltrials.gov/show/NCT01590056

Trefwoorden

  1. 17-01-19 17-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

17 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Parkinson's Disease NCT01590056

Eligibility Parkinson's Disease NCT01590056

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
clinically definite pd treated / candidates for treatment with dbs (patients with advanced idiopathic pd who are deemed appropriate for dbs surgery).
Beschrijving

ID.1

Datatype

boolean

patients will be included in the study irrespective of whether a diagnosis of major depression (mild to moderate but not severe mdd) is fulfilled at baseline. patients without depression will be monitored in the study for evidence of treatment emergent depression. patients with depression will be monitored for antidepressant effects of stimulation change.
Beschrijving

ID.2

Datatype

boolean

age 40-75 years
Beschrijving

ID.3

Datatype

boolean

male or female.
Beschrijving

ID.4

Datatype

boolean

competent and willing to give written informed consent.
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
significant suicidal risk [hamilton depression scale item 3 (suicide) >2].
Beschrijving

ID.6

Datatype

boolean

comorbidity with any psychotic disorder, bipolar disorder, post traumatic stress disorder (ptsd), eating disorder.
Beschrijving

ID.7

Datatype

boolean

lifetime history of substance or alcohol dependence or of abuse in the preceding 12 months
Beschrijving

ID.8

Datatype

boolean

significant cognitive decline, as measured by addenbrooke's cognitive examination (ace) and the frontal assessment battery (fab).
Beschrijving

ID.9

Datatype

boolean

Similar models

Eligibility Parkinson's Disease NCT01590056

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
clinically definite pd treated / candidates for treatment with dbs (patients with advanced idiopathic pd who are deemed appropriate for dbs surgery).
boolean
ID.2
Item
patients will be included in the study irrespective of whether a diagnosis of major depression (mild to moderate but not severe mdd) is fulfilled at baseline. patients without depression will be monitored in the study for evidence of treatment emergent depression. patients with depression will be monitored for antidepressant effects of stimulation change.
boolean
ID.3
Item
age 40-75 years
boolean
ID.4
Item
male or female.
boolean
ID.5
Item
competent and willing to give written informed consent.
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
significant suicidal risk [hamilton depression scale item 3 (suicide) >2].
boolean
ID.7
Item
comorbidity with any psychotic disorder, bipolar disorder, post traumatic stress disorder (ptsd), eating disorder.
boolean
ID.8
Item
lifetime history of substance or alcohol dependence or of abuse in the preceding 12 months
boolean
ID.9
Item
significant cognitive decline, as measured by addenbrooke's cognitive examination (ace) and the frontal assessment battery (fab).
boolean

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