ID

34259

Beschrijving

e-PAT Neuromod Evaluation of Personalized rTMS for Resistant Depression; ODM derived from: https://clinicaltrials.gov/show/NCT02410421

Link

https://clinicaltrials.gov/show/NCT02410421

Trefwoorden

  1. 16-01-19 16-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

16 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Depressive Disorder NCT02410421

Eligibility Depressive Disorder NCT02410421

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged from 18 to 65 y
Beschrijving

ID.1

Datatype

boolean

affiliated to the health insurance
Beschrijving

ID.2

Datatype

boolean

having signed an informed consent
Beschrijving

ID.3

Datatype

boolean

suffering from major depression according to the dsm5
Beschrijving

ID.4

Datatype

boolean

unresponsive or incomplete remission after at least one trial of antidepressant (> 6 weeks at efficient dose or side effects)
Beschrijving

ID.5

Datatype

boolean

treatment stable for > 6 weeks
Beschrijving

ID.6

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
contraindication for mri, rtms or tdcs: non-removable ferromagnetic body, prosthesis, pacemaker, medication delivered by an implanted pump clip or vascular stent, heart valve or ventricular shunt, seizure disorders, skin pathology in the region of tdcs electrode placement.
Beschrijving

ID.7

Datatype

boolean

pregnancy
Beschrijving

ID.8

Datatype

boolean

severe and non-stabilized somatic pathology
Beschrijving

ID.9

Datatype

boolean

patients deprived of liberty or hospitalized without their consent
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Depressive Disorder NCT02410421

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
aged from 18 to 65 y
boolean
ID.2
Item
affiliated to the health insurance
boolean
ID.3
Item
having signed an informed consent
boolean
ID.4
Item
suffering from major depression according to the dsm5
boolean
ID.5
Item
unresponsive or incomplete remission after at least one trial of antidepressant (> 6 weeks at efficient dose or side effects)
boolean
ID.6
Item
treatment stable for > 6 weeks
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
contraindication for mri, rtms or tdcs: non-removable ferromagnetic body, prosthesis, pacemaker, medication delivered by an implanted pump clip or vascular stent, heart valve or ventricular shunt, seizure disorders, skin pathology in the region of tdcs electrode placement.
boolean
ID.8
Item
pregnancy
boolean
ID.9
Item
severe and non-stabilized somatic pathology
boolean
ID.10
Item
patients deprived of liberty or hospitalized without their consent
boolean

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