Overweight and Obesity Clinical Trial
Official title:
The Effect of Olive Leaf Extract Administration on Cardiovascular Health
Verified date | May 2017 |
Source | Maastricht University Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to investigate the effects of daily supplementation of OLECOL for a period of 8 weeks on cardiovascular risk markers.
Status | Completed |
Enrollment | 80 |
Est. completion date | April 2017 |
Est. primary completion date | April 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Healthy individuals - Age between 18 and 70 years - Total cholesterol levels = 5.0 mmol/L - BMI 25-35 kg/m2 Exclusion Criteria: - History of severe cardiovascular, respiratory, urogenital, gastrointestinal/hepatic, hematological/immunologic, HEENT (head, ears, eyes, nose, throat). Dermatological/connective tissue, musculoskeletal, metabolic/nutritional, endocrine, neurological diseases, allergy, major surgery and /or laboratory assessments that might limit participation in or completion of the study protocol. - Diabetes - Use of medication that might have influence on endpoints (e.g. cholesterol lowering medication, hypertension medication) - Administration of investigational drugs or participation in any scientific intervention study which may interfere with this study in the 180 days prior to the study - Use of antibiotics in the 30 days prior to the start of the study - Use of antioxidants, minerals and vitamin supplements available in pharmacies, drugstores, food markets or in alternative medicine - Pregnancy, lactation - Abuse of products (> 20 alcoholic consumptions per week and drugs) - Smoking - Weight gain or loss (> 3 kg in previous 3 months) - High physical activity (>4.5 hours of running/week) - History of any side effects towards intake of olives |
Country | Name | City | State |
---|---|---|---|
Netherlands | Maastricht University Medical Center | Maastricht |
Lead Sponsor | Collaborator |
---|---|
Maastricht University Medical Center |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Blood lipid profile | 8 weeks | ||
Secondary | Lipid peroxidation | 8 weeks | ||
Secondary | Glucose metabolism | 8 weeks | ||
Secondary | Systolic and diastolic blood pressure | 8 weeks |
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