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Study of omega-3 supplements effects on treatment of patients with bipolar disorder

Study of use and non- use effects omega-3 supplements on treatment of patients with bipolar disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013112414333N12
Enrollment
100
Registered
2013-12-11
Start date
2013-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Bipolar disorder. Bipolar affective disorder

Interventions

Intervention 1: The intervention group received one omega-3 capsule (manufactured by Natures Factor company from America) daily for 3 months. Intervention 2: The control group was given 1000 mg placeb
Treatment - Drugs
Placebo
The intervention group received one omega-3 capsule (manufactured by Natures Factor company from America) daily for 3 months
The control group was given 1000 mg placebo daily for 3 months.

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Presence of bipolar disorders type I in mania phase or mixed based on DSM-IV. criteria, patient satisfaction and his head confirming to be treated by lithium and olanzapine. exclusion criteria: Mental retarded patients based on clinical diagnosis or IQ less than 70 using related tests; patients with pervasive developmental disorders based on history and clinical diagnosis; Patients requiring ECT or other treatments except lithium mood stabilizer (like other mood stabilizers) and olanzapine because of symptoms severity based on clinical assessment by a psychiatrist, drug abuse or drug dependence at least three months prior to the survey; pregnancy, the possibility of suicide, risk of harm to others; patients with severe complications of omega-3 usage such as disruption of bleeding time.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of illness. Timepoint: At baseline and 3 months after study. Method of measurement: Based on questionnaire.;Level of illness. Timepoint: At baseline and 3 months after study. Method of measurement: Based on questionnaire and at least 50% reduction in Yang scale.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026