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.
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
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.
- Conditions
- Bipolar Disorder
- 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 group | Role | What they receive |
|---|---|---|
| Lithium plus Fluoxetine Phase I | Other | All 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 I | Other | No participants began their participation on Lithium plus Placebo. Receives: Drug: Lithium / Placebo |
| Lithium plus Fluoxetine Phase II | Experimental | Patients 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 II | Placebo comparator | Patients 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.
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)
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
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
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.
- First posted19 Aug 2009 (estimated)
- Study start1 Jul 2009
- Primary completion1 Sep 2016
- Study completion1 Sep 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Bipolar DisorderStudies of the same condition, open and under way.
- More trials run by University of PennsylvaniaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- University of Pennsylvania
- Sponsor type
- University, hospital or other
- Collaborators
- National Institute of Mental Health (NIMH)
- Responsible party
- Sponsor
- Investigators
- Robert J. DeRubeis, PhD, Principal investigator, University of PennsylvaniaJohn M Zajecka, MD, Principal investigator, Rush University Medical Center
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
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 19 Oct 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Prevention of Relapse & Recurrence of Bipolar Depression
- ClinicalTrials.gov ID
- NCT00961961
- Acronym / sponsor ID
- R01MH080097
- Conditions
- Bipolar Disorder
- Keywords
- Bipolar Disorder, Manic Depression, Major Depressive Episode, Mania, Hypomania, Long Term Treatment
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 177 participants (actual)
- Lead sponsor
- University of PennsylvaniaUniversity, hospital or other
- Collaborators
- National Institute of Mental Health (NIMH)
- Study start
- 1 Jul 2009 (actual)
- Primary completion
- 1 Sep 2016 (actual)
- Study completion
- 1 Sep 2016 (actual)
- First posted
- 19 Aug 2009 (estimated)
- Results
- Posted 19 Oct 2020
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| Lithium plus Fluoxetine Phase I | Other | Drug: Lithium / FluoxetineAll 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. |
| Lithium plus Placebo Phase I | Other | Drug: Lithium / PlaceboNo participants began their participation on Lithium plus Placebo. |
| Lithium plus Fluoxetine Phase II | Experimental | Drug: Lithium / FluoxetinePatients who responded to Lithium plus Fluoxetine in Phase I and were randomized to continue on both compounds. |
| Lithium plus Placebo Phase II | Placebo comparator | Drug: Lithium / PlaceboPatients who responded to Lithium plus Fluoxetine in Phase I and were randomized to switch from Fluoxetine to placebo. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- 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
Key exclusion criteria (10 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Lithium / FluoxetineAlso: Lithium Carbonate / ProzacIndividualized Daily Dosage | Drug | Lithium plus Fluoxetine Phase I, Lithium plus Fluoxetine Phase II |
| Lithium / PlaceboAlso: Lithium Carbonate / Sugar PillIndividualized Daily Dosage | Drug | Lithium plus Placebo Phase I, Lithium plus Placebo Phase II |
Primary outcome
Number of Participants With Relapse of Major Depressive Episode Within 1 Year
Time frame: 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.
3 secondary outcomes
Number of Participants With an Onset of a Manic Episode Within 1 Year
Time frame: 1 Year
Number of Participants With an Onset of a Hypomanic Episode Within 1 Year
Time frame: 1 Year
Number of Participants With the Onset of a Sub-Syndromal Mood Conversion Episode Within 1 Year
Time frame: 1 Year
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Oct 2020.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- DeRubeis Lab Web PageLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Robert J. DeRubeis, PhD principal investigator
University of Pennsylvania
John M Zajecka, MD principal investigator
Rush University Medical Center
2 sites in 1 country: see every site and its status.
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.