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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00289484
Other study ID # 05156
Secondary ID
Status Recruiting
Phase Phase 2
First received February 7, 2006
Last updated September 11, 2006
Start date February 2006

Study information

Verified date September 2006
Source The University of New South Wales
Contact Catherine Owen, Bsc (hons)
Phone (02) 9382 3717
Email cath.owen@unsw.edu.au
Is FDA regulated No
Health authority Australia: Department of Health and Ageing Therapeutic Goods Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether augmentation of antidepressant medication with Omega-3 polyunsaturated fatty acids increases the speed and degree of improvement for patients with major depression


Description:

The study will be a 4 week, parallel-group double blind randomised control trial of the efficacy pf Omega-3 as an augmentor of antidepressant treatment for depression. People aged between 18 and 65 with a first or new episode of depression warranting treatment with antidepressant medication will be recruited. In addition to their antidepressant medication, participants will be randomly allocated to receive either Omega-3 (fish oil) or placebo (paraffin oil)for 4 weeks. Participants will commence treatment with the antidepressant and Omega-3/placebo simultaneously. Participants will be followed up at 1,3 and 4 weeks and will be asked to rate their mood daily for the 4 week study period. Blood samples will be taken pre and post treatment to measure change in Omega-3 levels.


Recruitment information / eligibility

Status Recruiting
Enrollment 52
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Participants must present with a first or new episode of DSM IV non-psychotic major depression warranting treatment with antidepressant mediation.

- Must be able to give informed consent.

Exclusion Criteria:

- History of psychosis or mania/hypomania or personality disorder.

- Non-English speaking or otherwise unable to provide historical information.

- Having taken Omega-3 dietary supplements in the last 3 months.

- History of allergy to Omega-3 supplements, finfish or shellfish.

- Pregnancy, breast feeding or plans to become pregnant during course of study.

- Post-natal depression

- Current drug or alcohol abuse or dependence or history of abuse or dependence over the last 12 months.

- Unstable thyroid function

- Hepatic or renal impairment or other medical conditions that may interfere with the absorption and metabolism of Omega-3 polyunsaturated fatty acids

- Coagulopathy or anticoagulant treatment due to theoretical bleeding risk.

- Patients who, in the investigator's judgment pose a current serious suicidal or other safety risk, or patients who will not likely be able to comply with the study protocol.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Intervention

Drug:
Omega-3 Polyunsaturated Fatty Acids


Locations

Country Name City State
Australia The University of New South Wales/Black Dog Institute Sydney New South Wales

Sponsors (4)

Lead Sponsor Collaborator
The University of New South Wales Ocean Nutrition, Sphere Healthcare, Your Health Inc.

Country where clinical trial is conducted

Australia, 

References & Publications (2)

Parker G, Gibson NA, Brotchie H, Heruc G, Rees AM, Hadzi-Pavlovic D. Omega-3 fatty acids and mood disorders. Am J Psychiatry. 2006 Jun;163(6):969-78. Review. Erratum in: Am J Psychiatry. 2006 Oct;163(10):1842. — View Citation

Rees AM, Austin MP, Parker G. Role of omega-3 fatty acids as a treatment for depression in the perinatal period. Aust N Z J Psychiatry. 2005 Apr;39(4):274-80. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change form pretreatment score on Depression Rating scale at 4 weeks
Secondary Daily mood rating
Secondary Weekly measure of depression
Secondary Weekly measure of anxiety
Secondary Weekly measure of functional status
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