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CompletedNCT00010868Updated Aug 18, 2006

Omega-3 Fatty Acids in Bipolar Disorder

A Phase 2 interventional study of Omega-3 Fatty Acids in Bipolar Disorder, sponsored by National Center for Complementary and Integrative Health (NCCIH). Completed at 2 sites in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2006-08-18.

Sponsored by National Center for Complementary and Integrative Health (NCCIH) · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Ages
18 Years to 65 Years
Sex
All
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Study summary

This is a 12 month study of omega-3 fatty acids in bipolar disorder. This study will be a 12-month, parallel group, double-blind comparison of the prophylactic efficacy of omega-3 fatty acids vs. placebo in 120 bipolar I patients. All subjects entering the primary prophylactic study will be euthymic or have only subsyndromal mood symptoms for at least 4 weeks. In addition, their concomitant medication (only lithium, divalproex, or no medication will be permitted) will also be stable and at accepted therapeutic levels for at least 4 weeks. An 8-week lead-in phase will be available to subjects who do not meet the current symptom and concomitant medication inclusion criteria (however, subjects must meet all of the other inclusion/exclusion criteria): 1. 4 weeks of euthymic or subsyndromal mood. 2. Subjects who are not already receiving lithium or divalproex. 3. Subjects receiving other psychotropic medications.

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Conditions studied

  • Bipolar Disorder

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Keywords

  • bipolar disorder
  • omega-3 fatty acids
  • eicosapentaenoic acid
  • docosahexaenoic acid
03

In context

Bipolar Disorder

1,601 studies on the registry are indexed under Bipolar Disorder; 255 are open to participants now.

Browse Bipolar Disorder studies →

Lead sponsor

National Center for Complementary and Integrative Health (NCCIH) is the lead sponsor of 218 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Meet DSM-IV criteria for bipolar disorder, type I.
  • Have had an episode of mania, hypomania, mixed mania, or major depression within the preceding 12 months, as defined by SCID criteria.
  • Able to give informed consent.

Exclusion criteria

Exclusion Criteria:

  • Patients with significant medical co-morbidity, such as active hepatic or renal disease, any type of coagulopathy, lipidoses, dementia, history of significant head injury, active cancer or cancer treatment, or other medical problems which may interfere with the absorption and metabolism of omega-3 fatty acids. In addition, any medical disorder with symptoms (e.g. aphasia, encephalopathy, etc.) which would make it difficult to determine the clinical response to the study drugs.
  • Patients with significant psychiatric co-morbidity, such as another currently active Axis 1 or 2 disorder requiring treatment. Patients with other, active mental disorders may have psychiatric symptoms that would make it difficult to assess mood response to the study drugs. For example, a patient with significant anxiety or panic symptoms requiring medication would be excluded, whereas a patient with past or currently very mild anxiety symptoms not requiring active treatment would be eligible.
  • Patients receiving Coumadin, or other drugs with strong effects on coagulation will be excluded due to the theoretical increased risk of bleeding on omega-3 fatty acid therapy. Low dose or intermittent NSAIDs will be permitted.
  • Patients receiving drugs which affect lipid metabolism, such as HMG CoA inhibitors, high-dose niacin, gemfibrozil, and others.
  • Pregnant patients - due to the unknown effects of high dose omega-3 fatty acids on the fetus.
  • Patients who, in the investigator's judgment pose a current serious suicidal or homicidal risk, or patients who will not likely be able to comply with the study protocol.
  • Bipolar patients receiving clozapine. These patients will be excluded due to the likelihood of extreme treatment resistance in clozapine-treated bipolar disorder. It may be unwise to discontinue the patient's clozapine, since recurrence may occur. Also, based on uncontrolled data, clozapine may be a uniquely effective mood stabilizer, which would add a potential confound to the study.
  • Patients who meet DSM-IV criteria for substance abuse within 1 month of this trial or substance dependence within 3 months.
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Study design

Phase
Phase 2
Primary purpose
Treatment
Intervention model
Parallel assignment
Masking
Double

Interventions

  • DrugOmega-3 Fatty Acids
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Study locations

2 sites
  • McLean Hospital
    Belmont, Massachusetts 02478, United States
  • Baylor College of Medicine
    Houston, Texas 77030, United States
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References and documents

Publications

  • Stoll AL, Severus WE, Freeman MP, Rueter S, Zboyan HA, Diamond E, Cress KK, Marangell LB. Omega 3 fatty acids in bipolar disorder: a preliminary double-blind, placebo-controlled trial. Arch Gen Psychiatry. 1999 May;56(5):407-12. doi: 10.1001/archpsyc.56.5.407. PubMed 10232294 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 18, 2006, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00010868
Lead sponsor
National Center for Complementary and Integrative Health (NCCIH)
Collaborators
Pronova BioPharma
First posted
Feb 5, 2001
Start date
Jul 2000
Completion
Jul 2004
Last update
Aug 18, 2006

Study contacts

Andrew L. Stoll, M.D.
principal investigator · Mclean Hospital
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2006. You cannot join it, but the record below documents what was studied.

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