Hypercholesterolemia Clinical Trial
— DESCOOfficial title:
Randomized Clinical Trial, Controlled Against Placebo, Performed to Evaluate the Effect of a Phytosterol-based Product (2.5 g/Day), After 3 Weeks of Intake, on the Lipid Profile, Also in Relation to the Quality of the Diet, in Subjects With Moderate Hypercholesterolemia and Low / Moderate Global Cardiovascular Risk
NCT number | NCT05265455 |
Other study ID # | DESCO_2021 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 1, 2021 |
Est. completion date | June 8, 2022 |
Verified date | January 2024 |
Source | University of Bologna |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
DESCO is a randomized clinical trial, controlled against placebo, performed to evaluate the effect of a phytosterol-based product (2.5 g/day), after 3 weeks of intake, on the lipid profile, also in relation to the quality of the diet, in subjects with moderate hypercholesterolemia and low / moderate global cardiovascular risk.
Status | Completed |
Enrollment | 50 |
Est. completion date | June 8, 2022 |
Est. primary completion date | June 8, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 65 Years |
Eligibility | Inclusion Criteria: - Total cholesterol plasma levels between 200 and 240 mg/dL and/or LDL cholesterol levels between 130 and 160 mg/dL - Triglyceride plasma levels <200 mg / dL - Cardiovascular risk at 10 years (according to the SCORE algorithm) <5%. - Signature of the informed consent form Exclusion Criteria: - Subjects in secondary prevention for cardiovascular diseases or with a global cardiovascular risk (according to the SCORE algorithm) > 5% at 10 years - Triglyceride plasma levels >200 mg / dL - Decompensated diabetes - Alcoholism - Food allergy - Recent intake of functional foods or supplements for cholesterol control - Intake of lipid-lowering drugs or drugs affecting lipid metabolism in the last 2 months - Alterations in thyroid, hepatic or renal function (transaminases greater than 3 times the maximum values; glomerular filtration rate <30ml / min), muscle diseases, even if subclinical - Obesity (BMI> 30) - Any medical or surgical condition that could make the patient's adherence to the study protocol complex or inconstant. |
Country | Name | City | State |
---|---|---|---|
Italy | S. Orsola-Malpighi University Hospital | Bologna |
Lead Sponsor | Collaborator |
---|---|
University of Bologna |
Italy,
Cicero AFG, Fogacci F, Giovannini M, Rizzoli E, Grandi E, D'Addato S, Borghi C. The Effect of Dietary Supplementation with Plant Sterols on Total and LDL-Cholesterol in Plasma Is Affected by Adherence to Mediterranean Diet: Insights from the DESCO Randomi — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Fasting lipid profile | Evaluation of the effects of the intake of phytosterols on fasting lipid profile, including the following parameters: total and LDL cholesterol, triglycerides, HDL cholesterol, plasma levels of apolipoproteinB-100. | 3 weeks | |
Secondary | Mediterranean index of the diet assessed by validated FFQ | Assessment of the relationship between the effects of the supplementation with phytosterols and the Mediterranean index of the diet assessed by using a validated food frequency questionnaire (Gnagnarella et al. Nutr Metab Cardiovasc Dis. 2018;28:1140-1147). | 3 weeks | |
Secondary | Weight | Evaluation of the effects of the intake of phytosterols on weight in kilograms | 3 weeks | |
Secondary | BMI | Evaluation of the effects of the intake of phytosterols on BMI (weight kilograms and height meters will be combined to report BMI in kg/m^2 ) | 3 weeks | |
Secondary | Abdominal circumference | Evaluation of the effects of the intake of phytosterols on abdominal circumference | 3 weeks | |
Secondary | Blood pressure | Evaluation of the effects of the intake of phytosterols on blood pressure | 3 weeks |
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