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Bipolar DisorderPhase 4NCT00961961

Prevention of Relapse & Recurrence of Bipolar Depression

A Phase 4 study testing Lithium / Fluoxetine in people with Bipolar Disorder, run by University of Pennsylvania at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to determine whether the long-term use of combined antidepressant plus mood stabilizer therapy is superior to mood stabilizer therapy alone in preventing the relapse and recurrence of bipolar depression. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Bipolar Disorder
What is being tested?
Lithium / Fluoxetine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
177 participants
Where
2 sitesUnited States
Study dates
1 Jul 2009to 1 Sep 2016
Phase
Phase 4
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Men/women (all races and ethnicity)
  • Age at least 18 years old
  • Bipolar Type I Disorder
  • Current Major Depressive Episode
  • Able to understand and provide signed informed consent

Who cannot join

  • Current alcohol or drug abuse
  • Alcohol or drug dependence within 3 months
  • Allergic to Fluoxetine or Lithium
  • Unstable medical condition (e.g., uncontrolled thyroid, renal, cardiovascular disease)
  • Pregnant or nursing women
  • Women of child-bearing potential unwilling to use a medically acceptable form of contraception
Show all 10Show fewer
  • Actively suicidal
  • Requiring hospitalization
  • Use of medication contraindicated with lithium or fluoxetine
  • Unable to participate in a year-long trial

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • Rush University Medical Center

    Chicago, Illinois, 60612

  • Depression Research Unit

    Philadelphia, Pennsylvania, 19104-3309

Other trials in United States

About this study

The purpose of this study is to determine whether the long-term use of combined antidepressant plus mood stabilizer therapy is superior to mood stabilizer therapy alone in preventing the relapse and recurrence of bipolar depression.

Read the detailed description

Recurrence of Bipolar I (BP I) major depressive episode (MDE), is now recognized as a major mental health problem. Recurrent BP I MDE is a disorder with no satisfactory therapy, and its treatment remains a challenge to clinicians. To date, initial and long-term therapy of BP I MDE has been based on un-validated practice guidelines. These guidelines recommend limiting antidepressant drug (AD) use during initial therapy of BP I MDE, and completely avoiding AD use during long-term therapy. There is, however, no empirical evidence to suggest that mood stabilizer (MS) monotherapy is superior to combined MS plus AD therapy in preventing recurrent BP I MDE. Nor is there evidence to suggest that long-term MS plus AD therapy results in more manic switch episodes. We present evidence that AD-induced mania during long-term therapy of BP I MDE has been over-estimated, and that long-term use of MS plus AD therapy may be superior to MS therapy alone in preventing recurrent BP I MDE. In this study, we will ask: "Does continuation therapy with combined lithium plus fluoxetine result in fewer MDE relapses and recurrences vs. lithium monotherapy?" To answer this question, patients with BP I MDE will receive combined lithium plus fluoxetine therapy for 8 weeks. Responders who stay well for an additional 4 weeks of consolidation therapy will then be randomized to double-blind continuation therapy with either (i) combined lithium plus fluoxetine, or (ii) lithium alone (following fluoxetine taper and discontinuation) for an additional 50 weeks. We hypothesize that long-term lithium plus fluoxetine therapy will result in fewer MDE relapses and recurrences vs. lithium monotherapy. We will also ask: "What is the relative safety, tolerability, and frequency of syndromal and sub-syndromal manic, hypomanic, and mixed state conversions during continuation treatment with combined lithium plus fluoxetine vs. lithium monotherapy?" To answer this question, we will measure: the frequency, severity, and duration of syndromal and sub-syndromal manic, hypomanic, and mixed state conversions; frequency, severity, and duration of treatment-emergent adverse events; frequency of treatment discontinuation; time to onset of first syndromal and sub-syndromal conversion event; time to first treatment intervention of each syndromal and sub-syndromal conversion event; and, time to onset of increase in suicidal ideation event. We hypothesize that lithium plus fluoxetine therapy will result in a similar frequency of syndromal and sub-syndromal conversion events, and a similar frequency of treatment-emergent adverse events. We further hypothesize that lithium plus fluoxetine therapy will result in fewer suicide ideation events and fewer study discontinuations vs. lithium monotherapy. We believe that the results of this trial may have an important public health impact on the current practice guidelines for treating BP I MDE.

Being tested
Lithium / Fluoxetine, Lithium / Placebo
Keywords
Bipolar Disorder, Manic Depression, Major Depressive Episode, Mania, Hypomania, Long Term Treatment
Medical subject headings
Bipolar Disorder, Mania

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Lithium / FluoxetineDrug

    Also called Lithium Carbonate / Prozac

    Individualized Daily Dosage

  • Lithium / PlaceboDrug

    Also called Lithium Carbonate / Sugar Pill

    Individualized Daily Dosage

Study groups in NCT00961961
Study groupRoleWhat they receive
Lithium plus Fluoxetine Phase IOtherAll participants were started in this arm. Those who met criteria for entry into Phase II were then randomized to one of the two Phase II arms.
Receives: Drug: Lithium / Fluoxetine
Lithium plus Placebo Phase IOtherNo participants began their participation on Lithium plus Placebo.
Receives: Drug: Lithium / Placebo
Lithium plus Fluoxetine Phase IIExperimentalPatients who responded to Lithium plus Fluoxetine in Phase I and were randomized to continue on both compounds.
Receives: Drug: Lithium / Fluoxetine
Lithium plus Placebo Phase IIPlacebo comparatorPatients who responded to Lithium plus Fluoxetine in Phase I and were randomized to switch from Fluoxetine to placebo.
Receives: Drug: Lithium / Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Participants With Relapse of Major Depressive Episode Within 1 Year

    Patients who were randomized to one of the Phase II conditions were interviewed once each month. If they met criteria for a relapse of a Major Depressive Episode, this was considered the study outcome. If they participated for the full year of Phase II without a documented relapse, they were considered a completer.

    Measured: 1 year

Secondary outcomes (3)
  1. Number of Participants With an Onset of a Manic Episode Within 1 Year

    Onsets of a manic episodes were ascertained with the clinician-rated Young Mania Rating Scale (YMRS). The YMRS covers 11 symptom groups over the previous 48 hours. Four of the items are rated on a scale from 0 to 4; the other 4 are rated on a scale of 0 to 8. A score of 12 or above indicates a manic episode.

    Measured: 1 Year

  2. Number of Participants With an Onset of a Hypomanic Episode Within 1 Year

    Onsets of a hypomanic episodes were ascertained with the clinician-rated Hypomania Interview Guide and associated scoring rules.

    Measured: 1 Year

  3. Number of Participants With the Onset of a Sub-Syndromal Mood Conversion Episode Within 1 Year

    Measured: 1 Year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Aug 2009 (estimated)
  2. Study start1 Jul 2009
  3. Primary completion1 Sep 2016
  4. Study completion1 Sep 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
177 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00961961
Sponsor's protocol ID
R01MH080097
Other IDs
R01MH080097, R01MH080098
Status last verified
Sep 2020
First submitted
18 Aug 2009
Last updated
19 Oct 2020
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Lithium / Fluoxetine in people with Bipolar Disorder, run by University of Pennsylvania at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Oct 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 19 Oct 2020). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Participants With Relapse of Major Depressive Episode Within 1 Year (time frame: 1 year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Oct 2020.

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