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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02052986
Other study ID # VCT-01
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received December 16, 2013
Last updated January 31, 2014

Study information

Verified date January 2014
Source New York Hospital Queens
Contact Brian S Marino, DO
Phone 814-404-4169
Email brm9071@nyp.org
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The investigators aim to test the hypothesis that dietary supplementation with VASCAZEN will correct omega-3 deficiency in cardiac rehab patients and improve biochemical risk factors.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult subjects (> or = 18 years of age)

- Enrolled in Cardiac Rehabilitation clinic with documented cardiovascular disease as assessed by the principle investigator

- Has had cardiovascular examination within the past 2 months

Exclusion Criteria:

- Subjects who refuse to provide written consent

- Subjects with medical conditions, as determined by the principal investigator, which prevented them from study participation

- Subjects with a known bleeding or clotting disorder

- Subjects with known allergies to fish

- Subjects with an implantable cardiac defibrillator

- Subjects with a heart transplant

- Female subjects who are currently taking hormone replacement therapy

- Subjects who are pregnant or planning on becoming pregnant

- Subjects currently taking Omega-3 fatty acid supplements (either under medical supervision or self-administered)

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
VASCAZEN
All enrolled subjects will receive 4 capsules daily of VASCAZEN which delivers 3.0 grams of EPA and DHA

Locations

Country Name City State
United States The NYHQ Cardiac Health Center Fresh Meadows New York

Sponsors (3)

Lead Sponsor Collaborator
New York Hospital Queens NYHQ Cardiac Health Center, Pivotal Therapeutics

Country where clinical trial is conducted

United States, 

References & Publications (11)

Albert CM, Campos H, Stampfer MJ, Ridker PM, Manson JE, Willett WC, Ma J. Blood levels of long-chain n-3 fatty acids and the risk of sudden death. N Engl J Med. 2002 Apr 11;346(15):1113-8. — View Citation

Bays H. Clinical overview of Omacor: a concentrated formulation of omega-3 polyunsaturated fatty acids. Am J Cardiol. 2006 Aug 21;98(4A):71i-76i. Epub 2006 May 30. Review. — View Citation

Derosa G (2011) Effects of n-3 PUFA on Insulin Resistance After an Oral Fat Load. European Journal of Lipid Science. 113: (8) 950-960

Dietary supplementation with n-3 polyunsaturated fatty acids and vitamin E after myocardial infarction: results of the GISSI-Prevenzione trial. Gruppo Italiano per lo Studio della Sopravvivenza nell'Infarto miocardico. Lancet. 1999 Aug 7;354(9177):447-55. Erratum in: Lancet 2001 Feb 24;357(9256):642. Lancet. 2007 Jan 13;369(9556):106. — View Citation

Geleijnse JM, Giltay EJ, Grobbee DE, Donders AR, Kok FJ. Blood pressure response to fish oil supplementation: metaregression analysis of randomized trials. J Hypertens. 2002 Aug;20(8):1493-9. — View Citation

Grimsgaard S, Bonaa KH, Hansen JB, Nordøy A. Highly purified eicosapentaenoic acid and docosahexaenoic acid in humans have similar triacylglycerol-lowering effects but divergent effects on serum fatty acids. Am J Clin Nutr. 1997 Sep;66(3):649-59. — View Citation

Harris WS, Von Schacky C. The Omega-3 Index: a new risk factor for death from coronary heart disease? Prev Med. 2004 Jul;39(1):212-20. — View Citation

Kris-Etherton PM, Harris WS, Appel LJ; American Heart Association. Nutrition Committee. Fish consumption, fish oil, omega-3 fatty acids, and cardiovascular disease. Circulation. 2002 Nov 19;106(21):2747-57. Erratum in: Circulation. 2003 Jan 28;107(3):512.. — View Citation

Mori TA, Burke V, Puddey IB, Watts GF, O'Neal DN, Best JD, Beilin LJ. Purified eicosapentaenoic and docosahexaenoic acids have differential effects on serum lipids and lipoproteins, LDL particle size, glucose, and insulin in mildly hyperlipidemic men. Am J Clin Nutr. 2000 May;71(5):1085-94. — View Citation

Thies F, Garry JM, Yaqoob P, Rerkasem K, Williams J, Shearman CP, Gallagher PJ, Calder PC, Grimble RF. Association of n-3 polyunsaturated fatty acids with stability of atherosclerotic plaques: a randomised controlled trial. Lancet. 2003 Feb 8;361(9356):477-85. — View Citation

von Schacky C, Harris WS. Cardiovascular risk and the omega-3 index. J Cardiovasc Med (Hagerstown). 2007 Sep;8 Suppl 1:S46-9. Review. — View Citation

* Note: There are 11 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Other Change in Omega-3 Score and Omega-3 Index Baseline, 6 weeks, 12 weeks No
Other Change in high-sensitivity C-reactive protein (hsCRP) Baseline, 6 weeks, 12 weeks No
Other Change in blood levels of total cholesterol, low-density lipoprotein (LDL), high density lipoprotein (HDL), very-low density lipoprotein (VLDL) cholesterol and their subfractions (particle size) Baseline, 6 weeks, 12 weeks No
Other Change in blood level of Triglycerides Baseline, 6 weeks, 12 weeks No
Other Change in fasting plasma glucose Baseline,12 weeks No
Other Change in blood glucose and insulin measurements following administration of oral glucose tolerance test (OGTT) Baseline, 12 weeks No
Other Change in glycated hemoglobin (HbA1c) Baseline,12 weeks No
Other Change in Lipoprotein associated Phospholipase (Lp-PLA2) Baseline, 6 weeks, 12 weeks No
Primary Change in sum of Omega-Score and Omega-Index Change in the sum of the subject's blood Eicosapentaenoic acid (EPA) + Docosahexaenoic acid (DHA) + Docosapentaenoic acid (DPA) levels (Omega-Score) and the change in the sum of the subject's red blood cell (RBC) EPA + DHA levels (Omega-Index) over 12 weeks of study treatment with Vascazen 12 weeks No
Secondary Change in patient health questionnaire-9 (PHQ-9) depression scale Change in patient health questionnaire-9 (PHQ-9) depression scale after 12 weeks of study treatment 12 weeks No
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