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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01371383
Other study ID # DOH94F044
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2006
Est. completion date August 31, 2015

Study information

Verified date November 2023
Source National Science Council, Taiwan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The whole study will be divided into two major parts: (A) A 12-week, double-blind, randomized controlled, parallel n-3 fatty acids adjunctive therapy study in 30 bipolar disorder patients with mild to moderate depression. (B) A double-blind, randomized controlled, parallel n-3 fatty acid add-on prophylactic study in 31 patients with stable bipolar disorder.


Description:

Part of the study will be a 12-week parallel-group placebo-controlled double-blind randomized n-3 fatty acids add-on combination therapy trial. A total of 30 patients in the acute depression stage of bipolar disorder will be collected from outpatient clinics and randomly assigned to receive n-3 fatty acids or placebo. T-test (or Mann-Whitney U-Test) will be used to evaluate the differences in the severity of depressive and manic symptoms between the two groups across the study points. The second part of the study will be a 6-month add-on prophylactic trial with parallel-group, double-blind random allocation to n-3 fatty acids or placebo groups. A total of 31 patients with stable bipolar disorder recruited by newspaper advertisements will be recruited and randomly assigned to receive n-3 fatty acids or a placebo. Kaplan-Meier Survival analysis will be used to evaluate the differences in the recurrence rate of bipolar depression between the two groups. Also, t-test (or Mann-Whitney U-Test) will be used to evaluate the differences in the severity of depressive and manic symptoms between the two groups across the study points. The 2 separate studies will be conducted after approval from the Human Trials Committee.


Recruitment information / eligibility

Status Completed
Enrollment 61
Est. completion date August 31, 2015
Est. primary completion date May 31, 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. DSM-IV criteria for bipolar disorder. 2. Age being age 18-65. 3. Capacity and willingness to give written informed consent. 4. Routine biochemical parameters within normal range. Exclusion Criteria: 1. Presence of any major medical illnesses. 2. Recent or past history of other DSM-IV axis I diagnoses such as psychotic disorders, organic mental disorders, substance abuse, substance dependence and anxiety disorder; acute psychotic state or strong suicidal attempts; and DSM-IV axis-II diagnoses, including borderline and antisocial personality disorder.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
n-3 fatty acids
EPA 1680 mg/d + DHA 880 mg/d
placebo
Soybean oil

Locations

Country Name City State
Taiwan China Medical University Hospital Taichung

Sponsors (1)

Lead Sponsor Collaborator
National Science Council, Taiwan

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in HRSD-21 scores Differences in depression severity based on the Hamilton Rating Scale for Depression 21 (HRSD) across the study points. Weeks 0, 1, 2, 4, 6, 8, and 12
Primary Differences in recurrence rate of bipolar depression Differences in the rate of recurrence of bipolar disorder between the patients in the n-3 group and placebo group across the study points. From 0 to 6 months
Secondary Changes in Young Mania Rating Scale scores Changes in Young Mania Rating Scale scores across the time points in the study Weeks 0, 1, 2, 4, 6, 8, and 12
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