ID

30520

Descrizione

Combination Deplin® and Antidepressant Therapy for a Major Depressive Episode (MDE)- a Retrospective Analysis; ODM derived from: https://clinicaltrials.gov/show/NCT01001559

collegamento

https://clinicaltrials.gov/show/NCT01001559

Keywords

versioni (1)
  1. 11/06/18 11/06/18 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

11 giugno 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Major Depressive Disorder NCT01001559

Inglese

Eligibility Major Depressive Disorder NCT01001559

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
males or females age 18-70
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
the active arm (arm #1) includes randomly selected 100-125 charts of patients with a primary diagnosis of major depression and a cgi-s of ≥4 who began deplin and ssri or snri therapy at the same time beginning in january 2007 to the present; and, control group (arm #2) includes randomly selected 125-150 charts of patients with a primary diagnosis of major depression who began ssri or snri therapy matched in severity (cgi-s of ≥4)
Descrizione

Arm Active | Major Depressive Disorder CGI - Severity of Illness | Deplin | SSRI | SNRIs | Control Group | Major Depressive Disorder CGI - Severity of Illness | SSRI | SNRIs

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1522541
UMLS CUI [1,2]
C0205177
UMLS CUI [2,1]
C1269683
UMLS CUI [2,2]
C3639887
UMLS CUI [3]
C1693359
UMLS CUI [4]
C0360105
UMLS CUI [5]
C1579361
UMLS CUI [6]
C0009932
UMLS CUI [7,1]
C1269683
UMLS CUI [7,2]
C3639887
UMLS CUI [8]
C0360105
UMLS CUI [9]
C1579361
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
folic acid >400 mcg taken at any time during the study
Descrizione

Folic Acid Dosage

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0016410
UMLS CUI [1,2]
C0178602
psychotic features in the current episode or a history of psychotic features
Descrizione

Feature Psychotic Depressive episode | Feature Psychotic

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C2348519
UMLS CUI [1,2]
C0033975
UMLS CUI [1,3]
C0349217
UMLS CUI [2,1]
C2348519
UMLS CUI [2,2]
C0033975
any bipolar disorder (current or past) or any psychotic disorder (current or past)
Descrizione

Bipolar Disorder | Psychotic Disorders

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0005586
UMLS CUI [2]
C0033975
current or past treatment with vagus nerve stimulation, ect, or transcranial magnetic stimulation
Descrizione

Vagus Nerve Stimulation | Electroconvulsive Therapy | Transcranial magnetic stimulation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2350432
UMLS CUI [2]
C0013806
UMLS CUI [3]
C0436548
antipsychotic therapy in conjunction with their antidepressant currently or in past 4 weeks
Descrizione

Antipsychotic drug therapy | Antidepressive Agents

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1319421
UMLS CUI [2]
C0003289
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Similar models

Eligibility Major Depressive Disorder NCT01001559

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
males or females age 18-70
boolean
C0001779 (UMLS CUI [1])
Arm Active | Major Depressive Disorder CGI - Severity of Illness | Deplin | SSRI | SNRIs | Control Group | Major Depressive Disorder CGI - Severity of Illness | SSRI | SNRIs
Item
the active arm (arm #1) includes randomly selected 100-125 charts of patients with a primary diagnosis of major depression and a cgi-s of ≥4 who began deplin and ssri or snri therapy at the same time beginning in january 2007 to the present; and, control group (arm #2) includes randomly selected 125-150 charts of patients with a primary diagnosis of major depression who began ssri or snri therapy matched in severity (cgi-s of ≥4)
boolean
C1522541 (UMLS CUI [1,1])
C0205177 (UMLS CUI [1,2])
C1269683 (UMLS CUI [2,1])
C3639887 (UMLS CUI [2,2])
C1693359 (UMLS CUI [3])
C0360105 (UMLS CUI [4])
C1579361 (UMLS CUI [5])
C0009932 (UMLS CUI [6])
C1269683 (UMLS CUI [7,1])
C3639887 (UMLS CUI [7,2])
C0360105 (UMLS CUI [8])
C1579361 (UMLS CUI [9])
Item Group
C0680251 (UMLS CUI)
Folic Acid Dosage
Item
folic acid >400 mcg taken at any time during the study
boolean
C0016410 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Feature Psychotic Depressive episode | Feature Psychotic
Item
psychotic features in the current episode or a history of psychotic features
boolean
C2348519 (UMLS CUI [1,1])
C0033975 (UMLS CUI [1,2])
C0349217 (UMLS CUI [1,3])
C2348519 (UMLS CUI [2,1])
C0033975 (UMLS CUI [2,2])
Bipolar Disorder | Psychotic Disorders
Item
any bipolar disorder (current or past) or any psychotic disorder (current or past)
boolean
C0005586 (UMLS CUI [1])
C0033975 (UMLS CUI [2])
Vagus Nerve Stimulation | Electroconvulsive Therapy | Transcranial magnetic stimulation
Item
current or past treatment with vagus nerve stimulation, ect, or transcranial magnetic stimulation
boolean
C2350432 (UMLS CUI [1])
C0013806 (UMLS CUI [2])
C0436548 (UMLS CUI [3])
Antipsychotic drug therapy | Antidepressive Agents
Item
antipsychotic therapy in conjunction with their antidepressant currently or in past 4 weeks
boolean
C1319421 (UMLS CUI [1])
C0003289 (UMLS CUI [2])
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