ID

13195

Descrizione

Neurophysiologic Monitoring of Antidepressant Treatment; ODM derived from: https://clinicaltrials.gov/show/NCT01360190

collegamento

https://clinicaltrials.gov/show/NCT01360190

Keywords

versioni (1)
  1. 23/01/16 23/01/16 -
Caricato su

23 gennaio 2016

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Major Depressive Disorder NCT01360190

Inglese

Eligibility Major Depressive Disorder NCT01360190

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
all subjects will meet dsm-iv criteria for major depression based upon the structured clinical interview for dsm-iv - patient version (scid-p) (first et al., 1994). all research personnel have undergone scid-p training, and soon will extend this training to the dsm-iv version.
Descrizione

major depression

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1269683
subjects also will have a score on the 17-item hamilton depression rating scale of > 18 (with item #1 > 2).
Descrizione

hamd

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0451203
all subjects will be under the care of a clinician not affiliated with the study at the time of entry into the study, and through the course of the study.
Descrizione

clinician care

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects will have no serious medical illness.
Descrizione

serious medical illness

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0009488
we will exclude patients also meeting criteria for the following groups of axis i diagnoses: delirium or dementia, substance-related disorders, schizophrenia or other psychotic disorders, or eating disorders.
Descrizione

axis i diagnoses

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0270287
UMLS CUI [2]
C0011206
UMLS CUI [3]
C0497327
UMLS CUI [4]
C0236969
UMLS CUI [5]
C0036341
UMLS CUI [6]
C0033975
UMLS CUI [7]
C0013473
in addition, patients meeting criteria for cluster a or b axis ii diagnoses will be excluded.
Descrizione

axis ii diagnoses

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0270288
subjects with a history of current or past active suicidal ideation, or suicide attempts will be excluded, as will patients who previously have failed to respond to an adequate clinical trial of fluoxetine, or have failed to tolerate the medication.
Descrizione

suicidal, fluoxetin response

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0438696
UMLS CUI [2]
C0016365
UMLS CUI [3]
C0521982
subjects who have had suboptimal trials, however, may still be considered for the study.
Descrizione

suboptimal trials

Tipo di dati

boolean

Ritorna all'inizio della pagina

Similar models

Eligibility Major Depressive Disorder NCT01360190

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
major depression
Item
all subjects will meet dsm-iv criteria for major depression based upon the structured clinical interview for dsm-iv - patient version (scid-p) (first et al., 1994). all research personnel have undergone scid-p training, and soon will extend this training to the dsm-iv version.
boolean
C1269683 (UMLS CUI [1])
hamd
Item
subjects also will have a score on the 17-item hamilton depression rating scale of > 18 (with item #1 > 2).
boolean
C0451203 (UMLS CUI [1])
clinician care
Item
all subjects will be under the care of a clinician not affiliated with the study at the time of entry into the study, and through the course of the study.
boolean
Item Group
C0680251 (UMLS CUI)
serious medical illness
Item
subjects will have no serious medical illness.
boolean
C0009488 (UMLS CUI [1])
axis i diagnoses
Item
we will exclude patients also meeting criteria for the following groups of axis i diagnoses: delirium or dementia, substance-related disorders, schizophrenia or other psychotic disorders, or eating disorders.
boolean
C0270287 (UMLS CUI [1])
C0011206 (UMLS CUI [2])
C0497327 (UMLS CUI [3])
C0236969 (UMLS CUI [4])
C0036341 (UMLS CUI [5])
C0033975 (UMLS CUI [6])
C0013473 (UMLS CUI [7])
axis ii diagnoses
Item
in addition, patients meeting criteria for cluster a or b axis ii diagnoses will be excluded.
boolean
C0270288 (UMLS CUI [1])
suicidal, fluoxetin response
Item
subjects with a history of current or past active suicidal ideation, or suicide attempts will be excluded, as will patients who previously have failed to respond to an adequate clinical trial of fluoxetine, or have failed to tolerate the medication.
boolean
C0438696 (UMLS CUI [1])
C0016365 (UMLS CUI [2])
C0521982 (UMLS CUI [3])
suboptimal trials
Item
subjects who have had suboptimal trials, however, may still be considered for the study.
boolean
Ritorna all'inizio della pagina 

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