ID

34259

Descripción

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

Link

https://clinicaltrials.gov/show/NCT02410421

Palabras clave

  1. 16/1/19 16/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

16 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Depressive Disorder NCT02410421

Eligibility Depressive Disorder NCT02410421

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged from 18 to 65 y
Descripción

ID.1

Tipo de datos

boolean

affiliated to the health insurance
Descripción

ID.2

Tipo de datos

boolean

having signed an informed consent
Descripción

ID.3

Tipo de datos

boolean

suffering from major depression according to the dsm5
Descripción

ID.4

Tipo de datos

boolean

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

ID.5

Tipo de datos

boolean

treatment stable for > 6 weeks
Descripción

ID.6

Tipo de datos

boolean

Exclusion Criteria
Descripción

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.
Descripción

ID.7

Tipo de datos

boolean

pregnancy
Descripción

ID.8

Tipo de datos

boolean

severe and non-stabilized somatic pathology
Descripción

ID.9

Tipo de datos

boolean

patients deprived of liberty or hospitalized without their consent
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Depressive Disorder NCT02410421

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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