ID

28922

Descrizione

Impact of Atypical Antipsychotic Therapy on Health Outcomes and Costs Among Patients With Major Depressive Disorder; ODM derived from: https://clinicaltrials.gov/show/NCT01145313

collegamento

https://clinicaltrials.gov/show/NCT01145313

Keywords

versioni (1)
  1. 16/02/18 16/02/18 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

16 febbraio 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Depressive Disorder, Major NCT01145313

Inglese

Eligibility Depressive Disorder, Major NCT01145313

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients who meet the following criteria will be included in the study:
Descrizione

Criteria Fulfill

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
aged 18 to 64 years
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
diagnosis of major depressive disorder during the study timeframe (icd 9 codes 296.2, 296.3, 311)
Descrizione

Major Depressive Disorder

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1269683
evidence of at least 6 consecutive claims for traditional antidepressant therapy with a 30 day supply or at least 2 claims with a 90 day supply (consecutive defined as ≤15 days gap)
Descrizione

Antidepressive Agents

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0003289
must be continually enrolled during the study timeframe and have both medical and pharmacy benefits
Descrizione

Enrollment Continuous

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1516879
UMLS CUI [1,2]
C0549178
evidence of at least 4 consecutive claims for an atypical antipsychotic prescription with a 30 day supply or 2 claims with a 90 day supply (consecutive defined as ≤15 days gap)
Descrizione

Atypical antipsychotic

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1276996
evidence of antidepressant therapy for at least 60 consecutive days prior to the initiation of atypical antipsychotic
Descrizione

Antidepressive Agents prior to Atypical antipsychotic

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0003289
UMLS CUI [1,2]
C0332152
UMLS CUI [1,3]
C1276996
after at least a 60 day trial of traditional antidepressant medications, patient augments with an atypical antipsychotic medication for at least 4 months.
Descrizione

Antidepressive Agents | Atypical antipsychotic Additional

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0003289
UMLS CUI [2,1]
C1276996
UMLS CUI [2,2]
C1524062
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients are excluded if they:
Descrizione

Criteria Fulfill

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
have any claims for a diagnosis of schizophrenia, schizoaffective or bipolar disorder during the study period
Descrizione

Schizophrenia | Schizoaffective Disorder | Bipolar Disorder

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0036341
UMLS CUI [2]
C0036337
UMLS CUI [3]
C0005586
have electroconvulsive therapy (ect) during the study period
Descrizione

Electroconvulsive Therapy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0013806
new augmentation with mood stabilizers, l-thyroxine (t4), l-thyronine (t3), buspirone, stimulant, or others during the post-period (table 1)
Descrizione

Mood Stabilizer | Thyroxine | Triiodothyronine | Buspirone | Stimulant

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2917435
UMLS CUI [2]
C0040165
UMLS CUI [3]
C0041014
UMLS CUI [4]
C0006462
UMLS CUI [5]
C0304402
are pregnant during the study period
Descrizione

Pregnancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
patients with medicare or medicaid
Descrizione

Patients Medicare | Patients Medicaid

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0018717
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C0025071
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Similar models

Eligibility Depressive Disorder, Major NCT01145313

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Criteria Fulfill
Item
patients who meet the following criteria will be included in the study:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Age
Item
aged 18 to 64 years
boolean
C0001779 (UMLS CUI [1])
Major Depressive Disorder
Item
diagnosis of major depressive disorder during the study timeframe (icd 9 codes 296.2, 296.3, 311)
boolean
C1269683 (UMLS CUI [1])
Antidepressive Agents
Item
evidence of at least 6 consecutive claims for traditional antidepressant therapy with a 30 day supply or at least 2 claims with a 90 day supply (consecutive defined as ≤15 days gap)
boolean
C0003289 (UMLS CUI [1])
Enrollment Continuous
Item
must be continually enrolled during the study timeframe and have both medical and pharmacy benefits
boolean
C1516879 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
Atypical antipsychotic
Item
evidence of at least 4 consecutive claims for an atypical antipsychotic prescription with a 30 day supply or 2 claims with a 90 day supply (consecutive defined as ≤15 days gap)
boolean
C1276996 (UMLS CUI [1])
Antidepressive Agents prior to Atypical antipsychotic
Item
evidence of antidepressant therapy for at least 60 consecutive days prior to the initiation of atypical antipsychotic
boolean
C0003289 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C1276996 (UMLS CUI [1,3])
Antidepressive Agents | Atypical antipsychotic Additional
Item
after at least a 60 day trial of traditional antidepressant medications, patient augments with an atypical antipsychotic medication for at least 4 months.
boolean
C0003289 (UMLS CUI [1])
C1276996 (UMLS CUI [2,1])
C1524062 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Criteria Fulfill
Item
patients are excluded if they:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Schizophrenia | Schizoaffective Disorder | Bipolar Disorder
Item
have any claims for a diagnosis of schizophrenia, schizoaffective or bipolar disorder during the study period
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
C0005586 (UMLS CUI [3])
Electroconvulsive Therapy
Item
have electroconvulsive therapy (ect) during the study period
boolean
C0013806 (UMLS CUI [1])
Mood Stabilizer | Thyroxine | Triiodothyronine | Buspirone | Stimulant
Item
new augmentation with mood stabilizers, l-thyroxine (t4), l-thyronine (t3), buspirone, stimulant, or others during the post-period (table 1)
boolean
C2917435 (UMLS CUI [1])
C0040165 (UMLS CUI [2])
C0041014 (UMLS CUI [3])
C0006462 (UMLS CUI [4])
C0304402 (UMLS CUI [5])
Pregnancy
Item
are pregnant during the study period
boolean
C0032961 (UMLS CUI [1])
Patients Medicare | Patients Medicaid
Item
patients with medicare or medicaid
boolean
C0030705 (UMLS CUI [1,1])
C0018717 (UMLS CUI [1,2])
C0030705 (UMLS CUI [2,1])
C0025071 (UMLS CUI [2,2])
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