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| ID | Type | Description | Link |
|---|---|---|---|
| NOPRODDEP4001 | Other Identifier | Johnson & Johnson Pte Ltd |
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| Name | Class |
|---|---|
| Elysia Group | UNKNOWN |
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The purpose of this study is to assess the epidemiology of Treatment Resistant Depression (TRD) in the nationally insured population in Taiwan including incidence, duration of clinical episodes, and prevalence by age and sex.
This is a retrospective study of approximately one million subjects randomly selected from an anonymized database National Health Insurance Research Database (NHIRD). Participants aged 18 years or older who have had neither a depression diagnosis nor a dispensing of an antidepressant medication in the last four months of 2004 will enter the study when they receive in 2005 a depression diagnosis and a dispensing of an antidepressant medication within 30 days of each other and will be followed up to 8 years or until they have 4 months with neither a depression diagnosis nor a dispensing of an antidepressant medication. Treatment Resistant Depression (TRD) Incidence, TRD prevalence by age and sex and duration of clinical episodes will be estimated.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Taiwan Participants with Treatment Resistant Depression | Taiwan participants with Depression will be followed up to 8 years for incidence and duration of treatment resistant depression. |
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| Measure | Description | Time Frame |
|---|---|---|
| Incidence Percentage of Participants with Treatment Resistant Depression | The percentage of beneficiaries of Taiwan's health insurance plan who developed treatment resistant depression during 2005 | Approximately 8 Years |
| Prevalence Percentage of Participants with Treatment Resistant Depression | Approximately 8 Years | |
| Duration of an episode of Depression | Time from onset of depression to cessation of depression visits and medications. | Approximately 8 Years |
| Measure | Description | Time Frame |
|---|---|---|
| Healthcare costs | Direct healthcare cost associated with depression treatment will be assessed. | Approximately 8 Years |
| Number of Participants With Comorbidities | Approximately 8 Years |
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Inclusion Criteria:
Exclusion Criteria:
- Participants who receive following diagnosis will be excluded, a) Mania, b) Schizophrenia (ICD-9 codes 295), c) Bipolar disorder (ICD-9 codes 296 bipolar-related), D) Dementia (ICD-9 codes 290 or 294); Note: Major depressive disorder (MDD) with psychotic behavior (ICD 296.24 for single episode, ICD 296.34 for recurrent episode) is not an exclusion
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Adults aged 18 and older are randomly sampled from the National Health Insurance Research Database (NHIRD).
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| Name | Affiliation | Role |
|---|---|---|
| Janssen Research & Development, LLC Clinical Trial | Janssen Research & Development, LLC | Study Director |
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| ID | Term |
|---|---|
| D061218 | Depressive Disorder, Treatment-Resistant |
| ID | Term |
|---|---|
| D003866 | Depressive Disorder |
| D019964 | Mood Disorders |
| D001523 | Mental Disorders |
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| Medications used by Participants with Treatment Resistant Depression | Approximately 8 Years |