Clinical trial

EFFECTS OF OLEUROPEIN ON BLOOD PARAMETERS AND INFLAMMATORY MARKERS IN ADULTS WITH METABOLIC SYNDROME

Active, not recruiting · Not applicable · 1 countries · Registry ID NCT06673914

Active, not recruitingNot applicableInterventional

What this study is about

The aim of this study is to determine the effect of 6 weeks supplementation of oleuropein on individuals diagnosed with metabolic syndrome. The baseline and end biochemical parameters and anthropometric measurements will be compared with control subjects.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to 49 Years

SexAll

Healthy volunteersNot accepted

ConditionMetabolic Syndrome, Insulin Resistance, Obesity, Abdominal, Obesity

Full registry criteria

Inclusion Criteria: * Individuals who volunteer to participate in the study by signing the voluntary consent form * Diagnosed with Metabolic Syndrome * Individuals who did not have any infection at the time the study started * Not consuming any medication * Not pregnant or lactating * Women aged 18-49 who have not entered menopause and men in the same age group * Willing to consume the given extract * Not allergic or intolerant to olive leaves * No history of drug use * People with a BMI below 40 kg/m2 Exclusion Criteria: * The patient included in the study leaves the study * Any health issues that may affect the results of the research during the research. * Occurrence of the problem and/or infection * Becoming pregnant during the research * Being in the experimental group and not consuming extract regularly * Failure to comply with the regulated medical nutrition treatment * Failure to participate in routine meetings and failure to complete necessary measurements * Starting to use any medication or nutritional supplement during the study * Leaving study voluntarily

Treatments and study arms

Control Group: Diet Group

Behavioral

Patient in "Diet Group" and "Oleuropein and Diet Group" will be given a personalized diet and be followed up by a dietician.

Oleuropein and Diet Group

Dietary Supplement

Dietary Supplement: Oleuropein (Olive Leaf Extract) Patients in "Oleuropein and Diet Group" will receive 200 mg/day oleuropein supplement and personalized diet followed up by a dietician.

Primary outcomes

Change from Baseline in the Fasting Blood Glucose (mg/dl) at 6 weeks6 weeks

The fasting blood glucose (mg/dl) at the baseline and 6 weeks later noted from the routinely requested tests in the hospital. These values recorded for all groups.

Change from Baseline in the Insulin (uU/mL) at 6 weeks6 weeks

The fasting blood glucose (mg/dl) at the baseline and 6 weeks later noted from the routinely requested tests in the hospital. These values recorded for all groups.

Change from Baseline in the Triglyceride (TG) (mg/dl), high density lipoprotein (HDL-C) (mg/dl), low density lipoprotein (LDL-C) (mg/dl), Total Cholesterol (mg/dl) at 6 weeks6 weeks

Triglyceride (TG) (mg/dl), high density lipoprotein (HDL-C) (mg/dl), low density lipoprotein (LDL-C) (mg/dl), Total Cholesterol (mg/dl) at the baseline and 6 weeks later noted from the routinely requested tests in the hospital. These values recorded for all groups.

Change from Baseline in the HOMA-IR at 6 weeks6 weeks

The fasting blood glucose (mg/dl) and fasting insulin (mU/L) values of the individuals with metabolic syndrome at the baseline and 6 weeks later noted from the routinely requested tests in the hospital. HOMA-IR calculated with the formula (fasting glucose (mg/dl) x fasting insulin (mU/L)) / 405. These values recorded for all groups.

Change from Baseline in the BMI (kg/m2)6 weeks

The body weight (kg) and height (m) of the individuals with metabolic syndrome were measured at the baseline and again after 6 weeks by the researcher, who noted the values in their files. The height of the patients was measured with a fixed height meter at 0.5 cm intervals, with shoes off. For body analysis, an 8-electrode bioelectrical impedance (BIA) device, Inbody 270, which performs segmental analysis, was used. Patients were asked to remove all metal items (rings, earrings, bracelets, watches, phones, etc.), any heavy clothing, shoes, and socks before stepping on the device. The device was set to -1.0 kg to account for the remaining clothes. From these measurements, body weight, body fat (kg), body fat percentage (%), body muscle (kg), and body water (kg) values were recorded. Body mass index (BMI) was calculated as weight (kg) divided by height (m) squared.

Change from Baseline in the Anthropometric Measurements6 weeks

The anthropometric measurements of the individuals with metabolic syndrome at the baseline and 6 weeks taken by the researcher and noted in their files. These measurements included waist circumference (cm), hip circumference (cm), mid-upper arm circumference (cm), waist-to-height ratio (cm), and waist-to-hip ratio (cm). Waist circumference was measured using an inflexible tape at the umbilicus level after normal exhalation to the nearest 0.1 cm. Hip circumference was measured from the widest area between the waist and the thigh. The waist-to-hip ratio was calculated using the formula waist (cm)/hip (cm), and the waist-to-height ratio was calculated using the formula waist (cm)/height (cm). Mid-upper arm circumference was measured on the left arm of the patients. Neck circumference was measured with the shoulders in a free position from the point where the thyroid cartilage was most prot…

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Atlas University🌐 Istanbul, Kağıthane, Turkey (Türkiye)

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