Informatie:
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ID
33636
Beschrijving
Neurobiological Changes When Treating Depression With Electroconvulsive Therapy - a Longitudinal Observational Study; ODM derived from: https://clinicaltrials.gov/show/NCT01869868
Link
https://clinicaltrials.gov/show/NCT01869868
Trefwoorden
Versies (1)
- 17-12-18 17-12-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
17 december 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Depression NCT01869868
Eligibility Depression NCT01869868
- StudyEvent: Eligibility
Similar models
Eligibility Depression NCT01869868
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Major Depressive Disorder
Item
major depressive disorder
boolean
C1269683 (UMLS CUI [1])
Depressive episode Bipolar Disorder
Item
depressive episode in bipolar disorder
boolean
C0349217 (UMLS CUI [1,1])
C0005586 (UMLS CUI [1,2])
C0005586 (UMLS CUI [1,2])
Age
Item
age 18 - 65 years
boolean
C0001779 (UMLS CUI [1])
Substance Dependence | Substance Use Disorders
Item
alcohol- and/or drug dependence or abuse in the past 3 months
boolean
C0038580 (UMLS CUI [1])
C0038586 (UMLS CUI [2])
C0038586 (UMLS CUI [2])
Disease Severe | Life threatening illness
Item
severe/life-threatening medical disease
boolean
C0012634 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C3846017 (UMLS CUI [2])
C0205082 (UMLS CUI [1,2])
C3846017 (UMLS CUI [2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent
Item
type i diabetes
boolean
C0011854 (UMLS CUI [1])
Neurodegenerative Disorder
Item
neurodegenerative disorder
boolean
C0524851 (UMLS CUI [1])
Informed Consent Unable
Item
inability to give written informed consent to participation in the study
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])
Medical contraindication Magnetic Resonance Imaging
Item
contradiction to mri scanning.
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,2])