ID

34240

Description

Study of Repetitive Transcranial Magnetic Stimulation (rTMS) as Adjuvant Treatment for Depression; ODM derived from: https://clinicaltrials.gov/show/NCT01115699

Lien

https://clinicaltrials.gov/show/NCT01115699

Mots-clés

  1. 15/01/2019 15/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

15 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Depression NCT01115699

Eligibility Depression NCT01115699

  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT01115699
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects whose depressive symptoms have not remitted during their participation in the "pharmacokinetics and pharmacodynamics of citalopram and escitalopram" study or the "pharmacokinetics and pharmacodynamics of duloxetine" study
Description

ID.1

Type de données

boolean

must be able to continue to take same dose of duloxetine through the course of the study
Description

ID.2

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
a history of failure for respond to electroconvulsive therapy (ect)
Description

ID.3

Type de données

boolean

any metal in the head (except in mouth)
Description

ID.4

Type de données

boolean

implanted medication pump or cardiac pacemaker
Description

ID.5

Type de données

boolean

have had prior brain surgery
Description

ID.6

Type de données

boolean

have unprovoked seizure disorder or family history of treatment resistant epilepsy
Description

ID.7

Type de données

boolean

pregnancy
Description

ID.8

Type de données

boolean

psychiatric hospitalization within the past two weeks
Description

ID.9

Type de données

boolean

suicide attempt with hospitalization within past three months
Description

ID.10

Type de données

boolean

Similar models

Eligibility Depression NCT01115699

  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT01115699
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
subjects whose depressive symptoms have not remitted during their participation in the "pharmacokinetics and pharmacodynamics of citalopram and escitalopram" study or the "pharmacokinetics and pharmacodynamics of duloxetine" study
boolean
ID.2
Item
must be able to continue to take same dose of duloxetine through the course of the study
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
a history of failure for respond to electroconvulsive therapy (ect)
boolean
ID.4
Item
any metal in the head (except in mouth)
boolean
ID.5
Item
implanted medication pump or cardiac pacemaker
boolean
ID.6
Item
have had prior brain surgery
boolean
ID.7
Item
have unprovoked seizure disorder or family history of treatment resistant epilepsy
boolean
ID.8
Item
pregnancy
boolean
ID.9
Item
psychiatric hospitalization within the past two weeks
boolean
ID.10
Item
suicide attempt with hospitalization within past three months
boolean

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