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Antidepressant Treatment of Melancholia in Late Life

Antidepressant Treatment of Melancholia in Late :Ife

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00000378
Enrollment
110
Registered
1999-11-03
Start date
1997-07-31
Completion date
2002-06-30
Last updated
2015-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

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.

Interventions

DRUGSertraline

12 week trial dose up to 200mgs

DRUGNortriptyline

12 week trial dose adjusted to therapeutic level

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
New York State Psychiatric Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to 95 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
HAMILTON Rating Scale for DEPRESSION RangeBASELINE COMPARED TO 12 WEEK MEASUREMENTHamilton 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

Countries

United States

Participant flow

Participants by arm

ArmCount
Sertaline
patients randomized to sertraline 12 week trial does up to 200mgs Sertraline: 12 week trial dose up to 200mgs
58
Nortriptyline
patients randomized to nortriptyline dose adjusted to therapeutic level Nortriptyline: 12 week trial dose adjusted to therapeutic level
52
Total110

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLack of Efficacy1614

Baseline characteristics

CharacteristicTotalSertalineNortriptyline
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
98 Participants50 Participants48 Participants
Age, Categorical
Between 18 and 65 years
12 Participants8 Participants4 Participants
Region of Enrollment
United States
110 participants58 participants52 participants
Sex: Female, Male
Female
64 Participants34 Participants30 Participants
Sex: Female, Male
Male
46 Participants24 Participants22 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
2 / 584 / 52
serious
Total, serious adverse events
0 / 580 / 52

Outcome results

Primary

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

Time frame: BASELINE COMPARED TO 12 WEEK MEASUREMENT

Population: intent to treat analysis

ArmMeasureGroupValue (MEAN)Dispersion
SertalineHAMILTON Rating Scale for DEPRESSION RangeBASELINE27.3 units on a scaleStandard Deviation 6.6
SertalineHAMILTON Rating Scale for DEPRESSION Range12 WEEK DATA10.7 units on a scaleStandard Deviation 8.3
NortriptylineHAMILTON Rating Scale for DEPRESSION RangeBASELINE27.1 units on a scaleStandard Deviation 4.4
NortriptylineHAMILTON Rating Scale for DEPRESSION Range12 WEEK DATA8.4 units on a scaleStandard Deviation 7.7
Comparison: logistic regression and mixed effects modelp-value: <0.05Regression, Logistic

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026