ID

34240

Descrição

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

Link

https://clinicaltrials.gov/show/NCT01115699

Palavras-chave

  1. 15/01/2019 15/01/2019 -
Titular dos direitos

see on clinicaltrials.gov

Transferido a

15 de janeiro de 2019

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Depression NCT01115699

Eligibility Depression NCT01115699

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

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
Descrição

ID.1

Tipo de dados

boolean

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

ID.2

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

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

ID.3

Tipo de dados

boolean

any metal in the head (except in mouth)
Descrição

ID.4

Tipo de dados

boolean

implanted medication pump or cardiac pacemaker
Descrição

ID.5

Tipo de dados

boolean

have had prior brain surgery
Descrição

ID.6

Tipo de dados

boolean

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

ID.7

Tipo de dados

boolean

pregnancy
Descrição

ID.8

Tipo de dados

boolean

psychiatric hospitalization within the past two weeks
Descrição

ID.9

Tipo de dados

boolean

suicide attempt with hospitalization within past three months
Descrição

ID.10

Tipo de dados

boolean

Similar models

Eligibility Depression NCT01115699

  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT01115699
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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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