Study Comparing Remission Rates, in Patients With Major Depressive Disorder (MDD)
NCT00770289
ABOUT THIS STUDY
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- Outpatients
- 18-75 years old
- Patients diagnosed with MDD according to DSM IV without psychotic symptoms
- HAM-D17 > or = 18 on inclusion
- Patients receiving treatment for the first time or changing treatment based on their doctor's decision
- Subjects with potentially problematic compliance
- Subjects participating in an interventional trial within the last 3 months
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Descriptive Information | ||||
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Brief Title | Study Comparing Remission Rates, in Patients With Major Depressive Disorder (MDD) | |||
Official Title | Open Label, Observational, Non-interventional Study for the Evaluation of Remission Rates in Patients With MDD Under Treatment With Various Anti-depressives | |||
Brief Summary | Tools known as 'depression scales 'are widely used as assessments to evaluate a patient's response to treatment. The purpose of this study is the evaluation of the remission rates for patients with MDD. The evaluation will involve the use of HAM-D 17, and HAM-D 7 questionnaires and the comparison of those questionnaires. | |||
Detailed Description | 12 weeks random | |||
Study Type | Observational | |||
Study Design | Observational Model: Cohort | |||
Target Follow-Up Duration | Not Provided | |||
Biospecimen | Not Provided | |||
Sampling Method | Probability Sample | |||
Study Population | Patients diagnosed with MDD who are either changing treatment or have never received treatment. | |||
Condition | Major Depressive Disorder | |||
Intervention | Other: Cohort
Cohort (Patients diagnosed with MDD who are either changing treatment or have never received treatment). | |||
Study Groups/Cohorts | Single group
Intervention: Other: Cohort | |||
Publications * | Not Provided | |||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. | ||||
Recruitment Information | ||||
Recruitment Status | Completed | |||
Actual Enrollment | 851 | |||
Original Estimated Enrollment | 1000 | |||
Actual Study Completion Date | December 2009 | |||
Actual Primary Completion Date | December 2009 (Final data collection date for primary outcome measure) | |||
Eligibility Criteria | Inclusion Criteria:
Exclusion Criteria:
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Sex/Gender |
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Ages | 18 Years to 75 Years (Adult, Older Adult) | |||
Accepts Healthy Volunteers | No | |||
Contacts | Contact information is only displayed when the study is recruiting subjects | |||
Listed Location Countries | Greece | |||
Removed Location Countries | ||||
Administrative Information | ||||
NCT Number | NCT00770289 | |||
Other Study ID Numbers | 0600B-102374 B2411003 ( Other Identifier: Pfizer ) | |||
Has Data Monitoring Committee | No | |||
U.S. FDA-regulated Product | Not Provided | |||
IPD Sharing Statement | Not Provided | |||
Responsible Party | Pfizer | |||
Study Sponsor | Pfizer | |||
Collaborators | Not Provided | |||
Investigators |
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PRS Account | Pfizer | |||
Verification Date | August 2012 |