ID

34240

Descrizione

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

collegamento

https://clinicaltrials.gov/show/NCT01115699

Keywords

  1. 15/01/19 15/01/19 -
Titolare del copyright

see on clinicaltrials.gov

Caricato su

15 gennaio 2019

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Depression NCT01115699

Eligibility Depression NCT01115699

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

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
Descrizione

ID.1

Tipo di dati

boolean

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

ID.2

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

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

ID.3

Tipo di dati

boolean

any metal in the head (except in mouth)
Descrizione

ID.4

Tipo di dati

boolean

implanted medication pump or cardiac pacemaker
Descrizione

ID.5

Tipo di dati

boolean

have had prior brain surgery
Descrizione

ID.6

Tipo di dati

boolean

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

ID.7

Tipo di dati

boolean

pregnancy
Descrizione

ID.8

Tipo di dati

boolean

psychiatric hospitalization within the past two weeks
Descrizione

ID.9

Tipo di dati

boolean

suicide attempt with hospitalization within past three months
Descrizione

ID.10

Tipo di dati

boolean

Similar models

Eligibility Depression NCT01115699

  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT01115699
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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