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Antidepressant Treatment of Melancholia in Late Life

Primary Purpose

Depression, Melancholia

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Sertraline
Nortriptyline
Sponsored by
New York State Psychiatric Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring Aged, Antidepressive Agents, Tricyclic, Depression, Female, Human, Male, Middle Age, Nortriptyline, Sertraline, Serotonin Uptake Inhibitors, Antidepressive Agents, Tricyclic -- *therapeutic use, Antidepressive Agents, Tricyclic -- adverse effects, Depression -- *drug therapy, Nortriptyline -- *therapeutic use, Nortriptyline -- adverse effects, Sertraline -- *therapeutic use, Sertraline -- adverse effects, Serotonin Uptake Inhibitors -- *therapeutic use, Serotonin Uptake Inhibitors -- adverse effects

Eligibility Criteria

60 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: - Patients must have: Unipolar major depression (per Diagnostic and Statistical Manuel-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.

Sites / Locations

  • 1051 Riverside Drive

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

sertaline

nortriptyline

Arm Description

patients randomized to sertraline 12 week trial does up to 200mgs

patients randomized to nortriptyline dose adjusted to therapeutic level

Outcomes

Primary Outcome Measures

HAMILTON Rating Scale for DEPRESSION Range
Hamilton scale range 0-40, values below 7 are considered normal. the higher the number the more severe the depression weekly assessments, The primary outcome is a comparison of the baseline Hamilton to the 12 week measurement

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
October 6, 2015
Sponsor
New York State Psychiatric Institute
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00000378
Brief Title
Antidepressant Treatment of Melancholia in Late Life
Official Title
Antidepressant Treatment of Melancholia in Late :Ife
Study Type
Interventional

2. Study Status

Record Verification Date
September 2008
Overall Recruitment Status
Completed
Study Start Date
July 1997 (undefined)
Primary Completion Date
June 2002 (Actual)
Study Completion Date
June 2002 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
New York State Psychiatric Institute
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief 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.
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 Diagnostic and Statistical Manuel-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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Melancholia
Keywords
Aged, Antidepressive Agents, Tricyclic, Depression, Female, Human, Male, Middle Age, Nortriptyline, Sertraline, Serotonin Uptake Inhibitors, Antidepressive Agents, Tricyclic -- *therapeutic use, Antidepressive Agents, Tricyclic -- adverse effects, Depression -- *drug therapy, Nortriptyline -- *therapeutic use, Nortriptyline -- adverse effects, Sertraline -- *therapeutic use, Sertraline -- adverse effects, Serotonin Uptake Inhibitors -- *therapeutic use, Serotonin Uptake Inhibitors -- adverse effects

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
110 (Actual)

8. Arms, Groups, and Interventions

Arm Title
sertaline
Arm Type
Active Comparator
Arm Description
patients randomized to sertraline 12 week trial does up to 200mgs
Arm Title
nortriptyline
Arm Type
Active Comparator
Arm Description
patients randomized to nortriptyline dose adjusted to therapeutic level
Intervention Type
Drug
Intervention Name(s)
Sertraline
Intervention Description
12 week trial dose up to 200mgs
Intervention Type
Drug
Intervention Name(s)
Nortriptyline
Other Intervention Name(s)
nortiptyline
Intervention Description
12 week trial dose adjusted to therapeutic level
Primary Outcome Measure Information:
Title
HAMILTON Rating Scale for DEPRESSION Range
Description
Hamilton scale range 0-40, values below 7 are considered normal. the higher the number the more severe the depression weekly assessments, The primary outcome is a comparison of the baseline Hamilton to the 12 week measurement
Time Frame
BASELINE COMPARED TO 12 WEEK MEASUREMENT

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: - Patients must have: Unipolar major depression (per Diagnostic and Statistical Manuel-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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven P. Roose, MD
Organizational Affiliation
New York State Psychiatric Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
1051 Riverside Drive
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

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Antidepressant Treatment of Melancholia in Late Life

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