ID

34259

Description

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

Lien

https://clinicaltrials.gov/show/NCT02410421

Mots-clés

  1. 16/01/2019 16/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

16 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Depressive Disorder NCT02410421

Eligibility Depressive Disorder NCT02410421

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged from 18 to 65 y
Description

ID.1

Type de données

boolean

affiliated to the health insurance
Description

ID.2

Type de données

boolean

having signed an informed consent
Description

ID.3

Type de données

boolean

suffering from major depression according to the dsm5
Description

ID.4

Type de données

boolean

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

ID.5

Type de données

boolean

treatment stable for > 6 weeks
Description

ID.6

Type de données

boolean

Exclusion Criteria
Description

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.
Description

ID.7

Type de données

boolean

pregnancy
Description

ID.8

Type de données

boolean

severe and non-stabilized somatic pathology
Description

ID.9

Type de données

boolean

patients deprived of liberty or hospitalized without their consent
Description

ID.10

Type de données

boolean

Similar models

Eligibility Depressive Disorder NCT02410421

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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