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Antidepressant Treatment of Melancholia in Late Life - Article


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Nortriptyline Oral Solution

Aventyl Oral Solution


Clinical Trial: Antidepressant Treatment of Melancholia in Late Life

This study is no longer recruiting patients.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)

Purpose

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.

Condition Treatment or Intervention
Depression
Melancholia
 Drug: Sertraline
 Drug: Nortriptyline

MedlinePlus related topics:  Depression;   Mental Health

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Parallel Assignment

Further Study Details: 

Study start: July 1997;  Study completion: June 2002

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

Ages Eligible for Study:  60 Years and above,  Genders Eligible for Study:  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.


      Location Information


      New York
            1051 Riverside Drive, New York,  New York,  10032,  United States

      Study chairs or principal investigators

      Steven P. Roose, MD,  Principal Investigator

      More Information

      Study ID Numbers:  MH55716
      Record last reviewed:  November 2004
      Last Updated:  November 15, 2004
      Record first received:  November 2, 1999
      ClinicalTrials.gov Identifier:  NCT00000378
      Health Authority: United States: Federal Government
      ClinicalTrials.gov processed this record on 2005-04-08


      Source: ClinicalTrials.gov
      Cache Date: April 8, 2005


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      August 29, 2008



      Page Updated: June 1, 2005
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