ID

33636

Description

Neurobiological Changes When Treating Depression With Electroconvulsive Therapy - a Longitudinal Observational Study; ODM derived from: https://clinicaltrials.gov/show/NCT01869868

Lien

https://clinicaltrials.gov/show/NCT01869868

Mots-clés

  1. 17/12/2018 17/12/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

17 décembre 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Depression NCT01869868

Eligibility Depression NCT01869868

  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT01869868
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
major depressive disorder
Description

Major Depressive Disorder

Type de données

boolean

Alias
UMLS CUI [1]
C1269683
depressive episode in bipolar disorder
Description

Depressive episode Bipolar Disorder

Type de données

boolean

Alias
UMLS CUI [1,1]
C0349217
UMLS CUI [1,2]
C0005586
age 18 - 65 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
alcohol- and/or drug dependence or abuse in the past 3 months
Description

Substance Dependence | Substance Use Disorders

Type de données

boolean

Alias
UMLS CUI [1]
C0038580
UMLS CUI [2]
C0038586
severe/life-threatening medical disease
Description

Disease Severe | Life threatening illness

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C3846017
pregnancy
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
type i diabetes
Description

Diabetes Mellitus, Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1]
C0011854
neurodegenerative disorder
Description

Neurodegenerative Disorder

Type de données

boolean

Alias
UMLS CUI [1]
C0524851
inability to give written informed consent to participation in the study
Description

Informed Consent Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
contradiction to mri scanning.
Description

Medical contraindication Magnetic Resonance Imaging

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485

Similar models

Eligibility Depression NCT01869868

  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT01869868
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
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])
Age
Item
age 18 - 65 years
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
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])
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])
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])
Medical contraindication Magnetic Resonance Imaging
Item
contradiction to mri scanning.
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])

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