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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03295708
Other study ID # MDD201610
Secondary ID
Status Recruiting
Phase N/A
First received September 18, 2017
Last updated October 6, 2017
Start date October 1, 2017
Est. completion date April 1, 2020

Study information

Verified date October 2017
Source Second Xiangya Hospital of Central South University
Contact Lu Wang, MD
Phone +8615116331768
Email luwang112@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this proposed study, the investigators will evaluate the effects of fish oil add-on in treatment of major depressive disorder(MDD).


Description:

Participants are randomly assigned to two groups (n=60): control (placebo, soybean) and fish oil (containing EPA 1440mg, DHA 960mg). The experimental groups will be compared to placebo to evaluate if it may benefit clinical symptoms, cognitive symptoms and metabolic markers in MDD patients. We also plan to investigate the changes in markers of inflammation at the same time.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date April 1, 2020
Est. primary completion date October 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

1. Able to provide informed consent

2. Men or women aged 18-50 years

3. A primary psychiatric diagnosis of major depressive disorder (MDD), by Diagnostic and Statistical Manual-5th ed (DSM-5) using the MINI

4. HAMD total score=21

5. No significantly modification of their diet from the time they sign consent to the end of study participation

Exclusion Criteria:

1. Suffering from other serious somatic diseases or comorbidities

2. Patients with serious nervous system disease

3. Patients in accordance with diagnostic standards of other mental illness

4. Patients who need to take benzodiazepine every day, and who currently need to be treated by electroconvulsive therapy or have received electroconvulsive therapy in the past 6 months

5. Pregnant women or lactating women, women with pregnancy plans during the trial period (12 months), women with a high risk of pregnancy but without taking any contraceptive measures

6. Patients with apparent suicide attempt or suicidal behavior

7. Any condition or medicines that may have an effect on biomarkers (within 1 week of the screening period or during whole trial period): long-term, regular use of NSAIDs, COX-2 inhibitors, immunosuppressant, steroids, interferon, chemotherapeutics, anticoagulants, malignancy, active autoimmune diseases, inflammatory bowel diseases, etc

8. Allergy history of PUFA

9. Intake of Fish oil more than 3g per day or eat fatty fish more than 3 times a week

Study Design


Intervention

Dietary Supplement:
fish oil capsule
N-3 PUFAs is a kind of essential fatty acid,however the formation is too slow. Studies show that intakes of N-3 PUFAs is associated with MDD.It have to be got from food like deep-sea fishes. EPA and DHA are crucial for the body.Although studies have shown that reduced N-3 PUFAs were correlated with MDD, and patients with an elevated rate of N-6 PUFAs /N-3 PUFAs or a low level of DHA may be at higher odds for suicide. Trials on whether N-3 PUFAs is effective in the treatment of MDD is still controversial, which might be affected by several factors, such as dose, duration etc.. Now there is no large-scale randomized controlled clinical trial in determining the effects of N-3 PUFAs add-on in treatment of MDD.
soybean oil capsule
placebo capsule

Locations

Country Name City State
China Mental Health Institute, Second Xiangya Hospital of Central South University Changsha Hunan

Sponsors (2)

Lead Sponsor Collaborator
Second Xiangya Hospital of Central South University Xiangya Hospital of Central South University

Country where clinical trial is conducted

China, 

References & Publications (9)

Appleton KM, Rogers PJ, Ness AR. Updated systematic review and meta-analysis of the effects of n-3 long-chain polyunsaturated fatty acids on depressed mood. Am J Clin Nutr. 2010 Mar;91(3):757-70. doi: 10.3945/ajcn.2009.28313. Epub 2010 Feb 3. Review. — View Citation

Bloch MH, Hannestad J. Omega-3 fatty acids for the treatment of depression: systematic review and meta-analysis. Mol Psychiatry. 2012 Dec;17(12):1272-82. doi: 10.1038/mp.2011.100. Epub 2011 Sep 20. Review. — View Citation

Freeman MP, Rapaport MH. Omega-3 fatty acids and depression: from cellular mechanisms to clinical care. J Clin Psychiatry. 2011 Feb;72(2):258-9. doi: 10.4088/JCP.11ac06830. Review. — View Citation

Kessler RC, Birnbaum H, Bromet E, Hwang I, Sampson N, Shahly V. Age differences in major depression: results from the National Comorbidity Survey Replication (NCS-R). Psychol Med. 2010 Feb;40(2):225-37. doi: 10.1017/S0033291709990213. Epub 2009 Jun 17. — View Citation

Lalovic A, Klempan T, Sequeira A, Luheshi G, Turecki G. Altered expression of lipid metabolism and immune response genes in the frontal cortex of suicide completers. J Affect Disord. 2010 Jan;120(1-3):24-31. doi: 10.1016/j.jad.2009.04.007. — View Citation

McNamara RK, Carlson SE. Role of omega-3 fatty acids in brain development and function: potential implications for the pathogenesis and prevention of psychopathology. Prostaglandins Leukot Essent Fatty Acids. 2006 Oct-Nov;75(4-5):329-49. Epub 2006 Sep 1. Review. — View Citation

Monroe SM, Harkness KL. Recurrence in major depression: a conceptual analysis. Psychol Rev. 2011 Oct;118(4):655-74. doi: 10.1037/a0025190. Erratum in: Psychol Rev. 2011 Oct;118(4):674. — View Citation

Sprecher H. Metabolism of highly unsaturated n-3 and n-6 fatty acids. Biochim Biophys Acta. 2000 Jul 19;1486(2-3):219-31. Review. — View Citation

Xie L, Innis SM. Association of fatty acid desaturase gene polymorphisms with blood lipid essential fatty acids and perinatal depression among Canadian women: a pilot study. J Nutrigenet Nutrigenomics. 2009;2(4-5):243-50. doi: 10.1159/000255636. Epub 2010 Apr 15. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in Hamilton Depression Scale (HAMD) HAMD Subjects were evaluated for current depression with HAMD. W0 W4 W12 W24 W48
Secondary Changes in Clinical Global Impression (CGI) Subjects were evaluated for current severity of disease with CGI. W0 W4 W12 W24 W48
Secondary Changes in Hamilton Anxiety Scale (HAMA) Subjects were evaluated for current anxiety with HAMA. W0 W4 W12 W24 W48
Secondary Changes in Beck Depression Rating Scale (BDI) The BDI is a self-report inventory of depression symptom. W0 W4 W12 W24 W48
Secondary Changes in Self-Rating Anxiety Scale (SAS) The SAS is a self-report inventory of anxiety symptom. W0 W4 W12 W24 W48
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