Antidepressant Treatment of Melancholia in Late Life
Information source: National Institute of Mental Health (NIMH)
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Depression; Melancholia
Intervention: Sertraline (Drug); Nortriptyline (Drug)
Phase: N/A
Status: Active, not recruiting
Sponsored by: National Institute of Mental Health (NIMH) Official(s) and/or principal investigator(s): Steven P. Roose, MD, Principal Investigator
Summary
The purpose of this study is to compare the safety and effectiveness of a select serotonin
re-uptake inhibitor (SSRI, sertraline) and a tricyclic antidepressant (TCA, nortriptyline) in
outpatients over the age of 60 who have major depression.
SSRIs are effective in the treatment of major depression. However, there is also evidence
that SSRIs may be significantly less effective than TCAs for patients with late-life major
depression with melancholia. Since SSRIs seem to be easier to take than TCAs and are more
widely prescribed, it is important to determine which of these types of antidepressants works
best to treat these patients.
Patients will be assigned randomly to receive either sertraline (a SSRI) or nortriptyline (a
TCA) for 12 weeks. Patients will be monitored for symptoms, side effects, and quality of
life. If a patient responds to treatment, he/she will participate in a 6-month continuation
phase in which he/she will continue to receive the same medication.
An individual may be eligible for this study if he/she:
Has unipolar major depression (with some exceptions) and is over 60 years old.
Clinical Details
Study design: Treatment, Randomized, Double-Blind, Parallel Assignment
Detailed description:
To compare the efficacy and safety of a select serotonin re-uptake inhibitor (SSRI,
sertraline) and a tricyclic antidepressant (TCA, nortriptyline) in outpatients over the age
of 60 who meet DSM-IV criteria for unipolar major depression, excluding patients who meet
criteria for psychotic or atypical subtype. To test the hypothesis that medication condition
interacts with diagnostic subtype (melancholic vs non-melancholic) in determining
antidepressant response. To examine the roles of symptom severity and alternative diagnostic
subtyping in contributing to this pattern.
SSRIs are effective in the treatment of major depression. However, there is also evidence
that SSRIs may be significantly less effective than TCAs for depressed patients with
melancholia. This issue is of particular concern in late-life major depression. SSRIs have
important safety advantages with respect to overdose and a benign cardiovascular profile.
Furthermore, the SSRIs do not have significant anticholinergic effects, and appear to be
better tolerated than the TCAs. Perhaps most important, the SSRIs currently are prescribed
widely as the medication treatment of first choice for major depression in late life.
Therefore, if it were determined that SSRIs are considerably less effective than TCAs in the
treatment of melancholia in the elderly, there would be significant ramifications for
clinical practice.
Randomization to sertraline (a SSRI) or nortriptyline (a TCA) is stratified by the presence
or absence of melancholia. Outcome measures for the 12-week acute phase include clinician and
patient ratings of symptoms, side effects, and an evaluation of the health-related quality of
life (HRQOL). At the end of the acute treatment phase, patients who meet criteria for
clinical response participate in a 6-month continuation phase.
Eligibility
Minimum age: 60 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
-
Patients must have:
Unipolar major depression (per DSM-IV criteria) with or without melancholia.
Exclusion Criteria:
-
Patients with the following symptoms or conditions are excluded:
Psychotic or atypical subtype of unipolar major depression.
Locations and Contacts
1051 Riverside Drive, New York, New York 10032, United States
Additional Information
Starting date: July 1997
Ending date: June 2002
Last updated: November 17, 2005
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