ID

34259

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT02410421

Nyckelord

  1. 2019-01-16 2019-01-16 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

16 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Depressive Disorder NCT02410421

Eligibility Depressive Disorder NCT02410421

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged from 18 to 65 y
Beskrivning

ID.1

Datatyp

boolean

affiliated to the health insurance
Beskrivning

ID.2

Datatyp

boolean

having signed an informed consent
Beskrivning

ID.3

Datatyp

boolean

suffering from major depression according to the dsm5
Beskrivning

ID.4

Datatyp

boolean

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

ID.5

Datatyp

boolean

treatment stable for > 6 weeks
Beskrivning

ID.6

Datatyp

boolean

Exclusion Criteria
Beskrivning

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.
Beskrivning

ID.7

Datatyp

boolean

pregnancy
Beskrivning

ID.8

Datatyp

boolean

severe and non-stabilized somatic pathology
Beskrivning

ID.9

Datatyp

boolean

patients deprived of liberty or hospitalized without their consent
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Depressive Disorder NCT02410421

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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