Depression
Conditions
Keywords
Depression
Brief summary
Phase III study evaluating Effexor XR in elderly patients with major depression.
Interventions
DRUGEffexor XR
Sponsors
Wyeth is now a wholly owned subsidiary of Pfizer
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients diagnosed with major depression based on DSM-IV-TR * Patients having minimal total score of 18 on the HAM-D17 and minimal score of 2 on the item of depressed mood of HAM-D at baseline
Exclusion criteria
* Patients with schizophrenia or any other psychotic disorder * Patients with history or presence of bipolar disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Response rate of HAM-D17 (Hamilton Rating Scale for Depression) at the final-on-therapy | — |
Secondary
| Measure | Time frame |
|---|---|
| Difference of total score of HAM-D17 between baseline and final-on-therapy | — |
| Remission rate of HAM-D17 at the final-on-therapy | — |
Countries
Japan
Outcome results
None listed