World Health Organization site
Skip Navigation Links

Main
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 October 2017
Main ID:  NCT00770289
Date of registration: 08/10/2008
Prospective Registration: No
Primary sponsor: Pfizer
Public title: Study Comparing Remission Rates, in Patients With Major Depressive Disorder (MDD) B2411003
Scientific title: Open Label, Observational, Non-interventional Study for the Evaluation of Remission Rates in Patients With MDD Under Treatment With Various Anti-depressives
Date of first enrolment: May 2008
Target sample size: 851
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT00770289
Study type:  Observational
Study design:   
Phase:  N/A
Countries of recruitment
Greece
Contacts
Name:     Pfizer CT.gov Call Center
Address: 
Telephone:
Email:
Affiliation:  Pfizer
Key inclusion & exclusion criteria

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



Age minimum: 18 Years
Age maximum: 75 Years
Gender: All
Health Condition(s) or Problem(s) studied
Major Depressive Disorder
Intervention(s)
Other: Cohort
Primary Outcome(s)
Percentage of Participants With Remission Based on Hamilton Depression Scale (HAM-D) [Time Frame: Week 12]
Secondary Outcome(s)
Number of Participants With Residual Symptoms in Case of Non Remission [Time Frame: Week 12]
Hamilton Depression Scale 17 (HAM-D17), HAM-D7 and Beck Depression Inventory (BDI) [Time Frame: Baseline, Week 12]
Percentage of Participants With Remission Based on Beck Depression Inventory (BDI) [Time Frame: Week 12]
Secondary ID(s)
0600B-102374
B2411003
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available: Yes
Date Posted: 31/08/2012
Date Completed:
URL: https://clinicaltrials.gov/ct2/show/results/NCT00770289
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.6 - Version history