Safety and Efficacy of Venlafaxine XR in Elderly Patients With Major Depression
Completed · Phase 4
Conditions studied: Depression
In brief
This research study is to evaluate the safety and usefulness of venlafaxine-XR in the treatment of major depression in the elderly.
Key facts
- Study ID
- NCT00177528
- Run by
- University of Pittsburgh
- People needed
- 70
- Starts
- 2000-10-01
- Last updated by the study team
- 2008-10-09
Who can join
Age: 60 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- men and women of all races who are 60 years old or older;
- a DSM-IV diagnosis of major depressive episode without psychotic features;
- 17-item Ham-D score of >15 for potential subjects who have not received any antidepressant treatment during this illness episode or HAM-D > 11 for potential subjects who have received treatment with an antidepressant (other than venlafaxine-XR) during this illness episode;
- a MMSE score of >15.
You may not qualify if…
- history of meeting DSM-IV criteria for mania, schizophrenia or other psychotic disorder;
- history of substance abuse or dependence, including alcohol, within the last three months;
- current hyponatremia (as defined as a serum sodium level < 130 meq/l);
- untreated or uncontrolled hypertension;
- a history of being unable to tolerate venlafaxine-XR or venlafaxine immediate release formulation;
- history of receiving venlafaxine-XR or venlafaxine immediate release formulation of 6 or more weeks at 300mg/d during index depressive episode; (7) EKG revealing QTc > 480 msec;
- myocardial infarction, unstable angina, palpitation or cardiogenic syncope within 3 months prior to entering this study;
- the presence of active suicidal ideation with intent.
Where it is running
- University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
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