Skip to main content
OpenTrials
Completed

NCT Number: NCT02644109

Effect On Serum Cholesterol Of Dairy Products With Addition Of Esterified Phytosterols

Hypercholesterolemia is an important risk factor for cardiovascular disease, asociated primarily with high plasma levels of LDL lipoprotein, which in turn depend on the endogenous hepatic synthesis of cholesterol and its absorption at intestinal level. It has been demonstrated that there reducing plasma LDL is beneficial, mainly with the use of statins, which are the first treatment option for a moderate hypercholesterolemia.

Phytosterols reduce the intestinal absorption of cholesterol by reducing its incorporation into lipid micelles. Consequently, phytosterols have become a relevant alternative treatment against low hypercholesterolemia. The target population are 40 to 65 years old individuals with low hypercholesterolemia.

Completed

Looking for future studies?

Notify Me

Key information

Age range

40 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Department of Nutrition, Diabetes and Metabolism. Pontificia Universidad Catolica de Chile, Santiago, Santiago Metropolitan, Chile

Loading trial locations.

About this study

Different protocols have demonstrated that phytosterol intake fluctuates between 1000 to 2000 mg per day decreasing LDL by around 10%, independently of levels of blood triglycerides and HDL (high density lipoproteins) concentrations. In fact, the National Cholesterol Education Program and the American Heart Association recommend the addition of 2 g/day of phytosterols to daily diet of adults. This is also recommended by the FDA (Food and Drug administration).

Phytosterols delivery has been proven effective when administrated in lipid matrixes such as margarines and dressings and low-fat such as skimmed milk and yogurt, proving to have an hypolipidemic effect. The investigational products consist of powder milk and a drinking yoghurt with the addition of esterified phytosterols, with a total daily intake of 1.95 g/day (1.17 g/day of free equivalent).

Primary objective: To evaluate the impact in Chilean population of phytosterols incorporated into dairy products in reduction of LDL cholesterol.

Secondary objectives:

  • To evaluate potential changes in blood cholesterol concentration according to nutritional state and age.
  • To determine the appearance of symptoms and/or effects during the intervention period.

The trial has been designed to evaluate the effect of phytosterols incorporated to low fat dairy products in Chile, through the consumption of one glass of milk powder and 90 mL of drinking yoghurt, which results in a daily consumption of 1.95 g/day of esterified phytosterols. This amount falls within demonstrated effective doses reported in literature.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Individuals between 40 to 65 y old.
  • Males and females.
  • Body mass index between 20 to 35 kg/m2
  • Mild hypercholesterolemia (LDL between 130 to 190 mg/dl) without requirement of immediate pharmacological treatment.
  • Without symptoms of atherosclerotic vascular disease.
  • Regular consumption of dairy foods (at least once a day).
  • Sedentary lifestyle defined as less than 20 min, three times per week of moderate to intense physical activity)

Exclusion criteria

  • Individuals with sitosterolemia.
  • Use of hypolipidemic drugs within the past 6 weeks before initiated the study.
  • Presence of type 1 or 2 diabetes; nephrotic syndrome or chronic kidney disease at stage III (estimated glomerular filtration rate<60 ml/min) or higher; gastrointestinal, liver, hepatobiliary, endocrine diseases or any condition potentially effecting lipid metabolism.
  • History of heart failure, unstable angina, cerebrovascular accident, heart failure, uncontrolled arrhythmias, high blood pressure (systolic>160 mm/Hg or diastolic>100 mm/Hg), cardiac surgery or other vascularization procedure.
  • Blood triglycerides higher than 400 mg/dl.
  • History of cancer disease over the last 5 years.
  • Pregnant and lactating women.
  • Lactose intolerant individuals or presence of related symptoms
  • Individuals with cow´s milk protein allergy.
  • Vegetarians
  • Regular use of drugs for obesity treatment, or affecting lipid metabolism.
  • Regular use of nutritional supplements.
  • Smokers having more than 5 units per day.
  • Individuals drinking more than 3 standard units per day of alcoholic beverages (>3 glasses of wine, 2 beers o 1 strong alcohol).

Treatment and study plan

phytosterol

Dietary Supplement

Day 1: Anthropometry, laboratory test, dietary intake (24 hour recall and food frequency questionnaire) and presence of symptoms and side effects will be determined, a logbook will be provided to record product consumption, symptoms, medications and side effects. Then will be randomly assigned to one of the groups.

Days 7 & 21: 24 hour recall, review of symptoms, side effects and adherence as registered in the logbook.

Days 15 & 30: Anthropometry, vital signs, venous blood sample, review of symptoms, side effects and adherence to intervention as registered on logbook, dietary intake (24-hour recall), delivery of monetary compensation proportional to the study days will be given before being discharged.

Other names: ACTICOL

Placebo

Dietary Supplement

Day 1: Anthropometry, laboratory test, dietary intake (24 hour recall and food frequency questionnaire) and presence of symptoms and side effects will be determined, a logbook will be provided to record product consumption, symptoms, medications and side effects. Then will be randomly assigned to one of the groups.

Days 7 & 21: 24 hour recall, review of symptoms, side effects and adherence as registered in the logbook.

Days 15 & 30: Anthropometry, vital signs, venous blood sample, review of symptoms, side effects and adherence to intervention as registered on logbook, dietary intake (24-hour recall), delivery of monetary compensation proportional to the study days will be given before being discharged.

Primary outcomes

  1. Serum LDL Cholesterol

    Time frame: 1 month

Sponsors and collaborators

Lead sponsor

University of Chile

Other

Collaborators

  • Pontificia Universidad Catolica de Chile

Registry information

Official study title

Effect On Serum Cholesterol Of Dairy Products With Addition Of Esterified Phytosterols In Chilean Subjects With Hypercholesterolemia

Acronym: ACTICOL

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Dec 31, 2015
Registry last updated
Sep 12, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.