Study Comparing Remission Rates, in Patients With Major Depressive Disorder (MDD)

NCT ID: NCT00770289

Last Updated: 2012-08-31

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

851 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-05-31

Study Completion Date

2009-12-31

Brief Summary

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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

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12 weeks random

Conditions

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Major Depressive Disorder

Study Design

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Observational Model Type

COHORT

Study Groups

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Single group

Cohort

Intervention Type OTHER

Cohort (Patients diagnosed with MDD who are either changing treatment or have never received treatment).

Interventions

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Cohort

Cohort (Patients diagnosed with MDD who are either changing treatment or have never received treatment).

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 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

Exclusion Criteria

* Subjects with potentially problematic compliance
* Subjects participating in an interventional trial within the last 3 months
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer Investigational Site

Haidari, Athens, Greece

Site Status

Pfizer Investigational Site

Haidari, Athens, Greece

Site Status

Pfizer Investigational Site

Ilissia, Athens, Greece

Site Status

Countries

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Greece

Related Links

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Other Identifiers

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B2411003

Identifier Type: OTHER

Identifier Source: secondary_id

0600B-102374

Identifier Type: -

Identifier Source: org_study_id