Prehypertension Clinical Trial
Official title:
Effect of Cardio Mato (Grade A Lyc-O-Mato, a Tomato Extracted Lycopene) on Blood Pressure and Serum Lycopene, Phytofluene, and Phytoene Levels in Pre-hypertensive Otherwise Healthy Subjects
Verified date | August 2012 |
Source | LycoRed Ltd. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The hypothesis of the study is that supplementation with Cardio Mato (a Tomato Extracted Lycopene)for 12 weeks will decrease the blood pressure of subjects with prehypertension compared to Placebo.
Status | Completed |
Enrollment | 80 |
Est. completion date | August 2013 |
Est. primary completion date | June 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Male and female subjects aged 18-65, both inclusive 2. Established Pre-hypertension defined as: Mean baseline SBP 130-139 mmHg and DBP of 89 mmHg or lower or SBP of 139 mmHg or lower and DBP of 85- 89 mmHg, at screening, eligibility and randomization visits 3. Subjects that did not receive any antihypertensive treatment in the past o present 4. Subjects that are willing to sign an informed consent form prior to joining the study Exclusion Criteria: 1. Subjects with Mean baseline SBP higher than 120 and lower than 130 mmHg 2. Subjects with Mean baseline DBP higher than 80 and lower than 85 mmHg 3. Subjects who are treated for blood pressure reduction (any treatment) 4. Subjects under treatment with other chronic medications (e.g. statins, NSAID etc.) 5. Subjects that use antioxidant agents or vitamins within 4 weeks prior to inclusion into the study 6. Subjects that will not be able to follow the study dietary proscriptions from the screening visit through the final visit 7. Subjects following any special diet including, but not limited to liquid, high or low protein, raw food, vegetarian or vegan, etc 8. Subjects with known allergy to tomatoes, carotenoids, or vitamin E 9. Subjects diagnosed with Diabetes Mellitus 10. Subjects suffering from obesity 11. Subjects Suffering from a clinically significant dyslipidaemia 12. Subjects suffering from cardiac disease; e.g. suffering from cardiac angina, subjects that were diagnosed with and MI, subjects that needed PTCA or CABG. Subjects diagnosed with LVH, CHF or valvular heart disease 13. Subjects diagnosed with PVD 14. Subjects who were diagnosed with Cerebrovascular disease, s/p CVA, TIA 15. Subjects who suffer from any kind of kidney disease 16. Subjects who suffer from chronic liver disease; defined as elevated AST and ALT at least by 2 times of the normal range 17. Subject with history or current use of illegal or "recreational" drugs 18. Subjects with a history of GI disease or surgery within 6 months prior to study inclusion 19. Subjects with a history of malignancy in the past 5 years 20. Subjects with a history of autoimmune disease |
Country | Name | City | State |
---|---|---|---|
Israel | Maccabi Health care, outpatient clinic | Holon |
Lead Sponsor | Collaborator |
---|---|
LycoRed Ltd. | Maccabi Healthcare Services, Israel |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Number of adverse events recorded during the supplementation period, lycopene compared to placebo | AE epizoda | 12 weeks | |
Primary | The effect Lyc-O-Mato on the blood pressure of pre-hypertensive otherwise healthy subjects compared to the placebo group following 12 weeks of treatment | Change in blood pressure from baseline to 12 weeks in mmHG | 12 weeks | |
Secondary | The effect Cardio Mato on the blood pressure of Pre-hypertensive otherwise healthy subjects compared to the placebo group following 4 and 8 weeks of treatment | Change in blood pressure from baseline to 4 and 8 weeks in mmHG | 4-8 weeks | |
Secondary | The correlation between B.P changes in the Cardio Mato or placebo treatment arms during the study with serum lycopene phytofluene, and phytoene levels | B.P change | 12 weeks |
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