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Treatment for Bipolar Depression: Acute & Prophylactic Efficacy With Citalopram

Treatment for Bipolar Depression: Acute & Prophylactic Efficacy With Citalopram

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00562861
Enrollment
119
Registered
2007-11-22
Start date
2007-11-30
Completion date
2014-07-31
Last updated
2017-03-24

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

Conditions

Bipolar Depression, Bipolar Disorder

Keywords

Bipolar Disorder, Bipolar Depression, Clinical Trials, Phase II, Clinical Pharmacology

Brief summary

Bipolar depression is one of the least studied depressive illnesses. The standard practice for many doctors is to use antidepressant medicines, but there are few studies on the long-term results of these medicines. The goal of this study is to look at how effective and safe these medicines are in treating bipolar depression when taken with a mood stabilizer medicine. The drug being studied is citalopram, also known as Celexa. Celexa is FDA approved for the treatment of major depression, but is not FDA approved for the treatment of bipolar depression. It is, however, standard practice for many doctors is to use antidepressants, like Celexa, to treat their patients with bipolar disorder depression. The drug will be studied in three ways. We will see if it helps treat depressive symptoms. We will see how the drug affects the brain using PET and fMRI scans. Finally, we will look at the possibility that there may be a gene that could predict if a person would get better taking the drug using genetics.

Detailed description

The problem of interest Depression is a common serious illness, with great personal suffering and a 10% or more risk of suicide. There are two kinds of depression, bipolar (depression alternating with mood swings) and unipolar (simple depression, or major depressive disorder). In both kinds of depression, antidepressants are commonly used. However, unlike unipolar depression, where a good deal of research supports this use, there is very little research on antidepressant use in bipolar disorder. Some studies support benefit with antidepressants for bipolar depression; i.e., if one is depressed, antidepressants can help a patient get better in the short-term. However, long-term studies are limited; the few available studies with older antidepressants did not demonstrate long-term preventive benefit. Some clinicians think new generation antidepressants (like Prozac and other serotonin reuptake inhibitors) are safer and more effective than the older antidepressants. Yet there are no rigorous long-term studies of new generation antidepressants in bipolar disorder. Recent observational studies with new antidepressants suggest that they may be harmful to some patients with bipolar disorder. Clinicians are thus left in a quandary. Antidepressants appear to be effective in the short term, but should the antidepressants (especially new generation antidepressants) be continued long-term? Some studies support both approaches. Importantly, some evidence exists that antidepressants can make many patients worse, with more and more depression or mania over time. This is a major public health problem, since clinicians prescribe antidepressants for the long-term in up to 80% of patients with bipolar disorder. This represents standard treatment, despite the limitations of the available evidence and the suggestion that in some patients such antidepressant use may be harmful. This study is also looking at possible biological predictors that may reflect an individual patients' likelihood that he or she will respond to a specific treatment. How the problem will be studied This project is one of the most rigorous studies of new generation antidepressants in long-term treatment of bipolar disorder. We will recruit patients with bipolar disorder who are currently in a depressive episode and are taking or eligible and interested in taking a mood stabilizer such as lithium. Subjects will then be randomly put into one of two groups. The first group will receive the generic antidepressant, citalopram while the other group will receive placebo, sugar pill. Patients will be closely followed and monitored by the research psychiatrist and through a series of safety labs. Subjects will have an MRI and PET scan for the biological predictors section of the study. The key question is: After the acute recovery, should they continue antidepressants or not? As there is limited scientific data, and opposing kinds of clinical experience, there is no clear rationale to making this decision. Our study seeks to provide a scientific basis for making that decision. We plan to follow subjects for a goal of 1 year to obtain long-term outcome data on which approach is best. How the research will advance scientific knowledge or human health Since there are no rigorous long-term studies with new generation antidepressants in bipolar disorder, this study will be a major advance in that knowledge. Clinicians will have some evidence on which to base that decision, rather than simply their own opinions or patients' preferences. In the light of recent evidence that antidepressants are potentially harmful to some patients, this study will provide more information about how new antidepressants work specifically for bipolar patients rather than unipolar depression (also known as major depression). The biological portion of the study will shed light on possible biological factors that could show how an individual may respond to a specific treatment. This could potentially help doctors to decide on which treatments are more or less likely to work for their individual patients rather then using a hit or miss type method.

Interventions

DRUGcitalopram + mood stabilizer

Citalopram dose will be flexibly designed, beginning at 10 mg/d for at least one week, and the increased by 10 mg per week to a maximum of 50 mg/d. No target dose will be provided but rather clinicians will dose to clinical efficacy. Thus the study will provide clinicians data on the effective dose if it is positive. The dose will not be predetermined at static amounts.

DRUGplacebo + mood stabilizer

This arm will only receive mood stabilizing medication. All subjects will be required to receive treatment with lithium, lamotrigine, valproate, or carbamazepine for at least one month at therapeutic blood levels or doses before randomization, or they must initiate one of these agents at study entry.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Tufts Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Current age ≥18 years * DSM-IV diagnosis of BPD, type-I, or type-II * Current major depressive episode using DSM-IV criteria, lasting 8 weeks or longer. * Use of lithium, divalproex, carbamazepine, or lamotrigine at therapeutic serum levels or doses for ≥4 weeks prior to study entry, or willingness to accept one of these agents. * Prior to initial evaluations, each subject must provide competent, written, informed consent.

Exclusion criteria

* Past non-response to a therapeutic trial of R,S-citalopram (≥100 mg/day for ≥8 weeks). * Previous intolerance of R,S-citalopram; * Diagnosis of unipolar depression * Diagnosis of schizoaffective disorder * Serious medical illness with acute instability (cardiac, respiratory, hepatic, renal), based on hospitalization in the past month * Abnormal thyroid function tests * Previous allergic reaction to or inability to tolerate lithium, divalproex, or carbamazepine at therapeutic serum levels. * Current or past renal dysfunction if taking lithium * Current or past hepatitis or other liver disease if taking divalproex * Current or past hematologic disease if on carbamazepine * Severe suicidal ideation, plan or intent, as documented by a score of ≥4 on the Montgomery Åsberg Depression Rating Scale suicidality item (Item 10). * Presence of psychosis * Cognitive impairment sufficient to impair ability to give informed consent. * Current pregnancy, or inability to utilize contraception * The presence of any metallic implants * History of claustrophobia

Design outcomes

Primary

MeasureTime frameDescription
MADRS Rating Scale Change6 weeksMontgomery Asberg Depression Rating scale assessed in mixed effects regression model. The total range for the scale is 0 to 60. Lower values involve less depression, while higher values involve worse depression. The change in the MADRS scale is interpreted as higher values meaning better outcomes, because more depressive symptoms are improved.

Countries

United States

Participant flow

Participants by arm

ArmCount
Mood Stabilizer Plus Citalopram
citalopram + mood stabilizer: Subjects receive the active drug, added to standard mood stabilizers.
60
Mood Stabilizer Plus Placebo
Placebo plus mood stabilizer: subjects receive placebo, added to standard mood stabilizers
59
Total119

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyAdverse Event11
Overall StudyLack of Efficacy55
Overall StudyLost to Follow-up73
Overall Studynoncompliance, moved72

Baseline characteristics

CharacteristicMood Stabilizer Plus CitalopramTotalMood Stabilizer Plus Placebo
Age, Continuous40.9 years
STANDARD_DEVIATION 12.6
41.5 years
STANDARD_DEVIATION 11.7
42.1 years
STANDARD_DEVIATION 11.3
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
1 Participants1 Participants0 Participants
Race (NIH/OMB)
Black or African American
21 Participants41 Participants20 Participants
Race (NIH/OMB)
More than one race
2 Participants6 Participants4 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
36 Participants71 Participants35 Participants
Region of Enrollment
United States
60 participants119 participants59 participants
Sex: Female, Male
Female
43 Participants74 Participants31 Participants
Sex: Female, Male
Male
17 Participants45 Participants28 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
23 / 6015 / 59
serious
Total, serious adverse events
1 / 600 / 59

Outcome results

Primary

MADRS Rating Scale Change

Montgomery Asberg Depression Rating scale assessed in mixed effects regression model. The total range for the scale is 0 to 60. Lower values involve less depression, while higher values involve worse depression. The change in the MADRS scale is interpreted as higher values meaning better outcomes, because more depressive symptoms are improved.

Time frame: 6 weeks

Population: All patients randomized were analyzed in intent to treat manner.

ArmMeasureValue (MEAN)Dispersion
CitalopramMADRS Rating Scale Change13.1 units on a scaleStandard Deviation 8.4
PlaceboMADRS Rating Scale Change15.2 units on a scaleStandard Deviation 9.9
p-value: 0.17Mixed Models Analysis

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026