Skip to content

Bioactivity of Olive Oils Enriched With Their Own Phenolic Compounds (VOHF1)

Bioavailability and Bioactivity of Olive Oils Enriched With Their Own Phenolic Compounds in a Dose-response Study (VOHF1)

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01347515
Acronym
VOHF1
Enrollment
12
Registered
2011-05-04
Start date
2011-04-30
Completion date
2011-09-30
Last updated
2011-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polyphenol Absorption in Healthy People

Keywords

Phenol-enriched olive oil, bioavailability, bioactivity

Brief summary

Hypothesis: A functional olive oil tailored to provide the best relationship between phenolic compounds (amount and type) phenolic bioavailability and bioactivity (antioxidant and anti-endothelial dysfunction) will be a useful tool for increasing not only circulating HDL cholesterol concentration, but also the functionality (antioxidant, anti-inflammatory, and reverse cholesterol transport capacity) of human HDL in vivo.

Detailed description

The first step is to determine, in healthy human subjects in postprandial condition, the best relationship between phenolic compounds (amount and type) / bioavailability and bioactivity (antioxidant, anti-inflammatory and anti-endothelial dysfunction) using olive oils enriched with its own broad-spectrum phenolic compounds.

Interventions

OTHERolive oil

Each volunteer will be given, in random order, a single dose of 30 ml on a base of 80 g bread, of the following functional olive oils (FOO): FOO750 ppm, FOO500 ppm, which are enriched with two different amounts of broad-spectrum phenolic compounds from the virgin FOO250 ppm; all prepared at the Universitat de Lleida. Post-ingestion the volunteers will rest for 8h in a comfortable warm room. During the run-in period of 2 weeks prior the first postprandial study and 1 week between each FOO treatment period, all subjects will undergo a 2-day pre-treatment wash-out period of a phenol-free diet (saturated fatty acids in the diet will be 10-13% of energy in an isocaloric diet). Volunteers will avoid non-essential physical activity during the 3 days prior to the treatment day.

Sponsors

Ministerio de Ciencia e Innovación, Spain
CollaboratorOTHER_GOV
Universitat de Lleida
CollaboratorOTHER
Fundacion IMIM
CollaboratorOTHER
University Rovira i Virgili
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy volunteers aged 20 to 70 years

Exclusion criteria

1. LDL cholesterol levels above 189 mg/dL 2. Triglycerides ≥350 mg/dL (the upper limit for correctly determining LDL-c by the Friedewald formula) 3. Physical examination and routine biochemical laboratory determinations will be carried out to exclude co-morbidities 4. Intake of antioxidant supplement or acetylsalicylic acid or any other drug with known antioxidative properties 5. Chronic alcoholism 6. Body mass index (BMI)≥30 kg/m2 7. Statin treatment prior to initiating the trial; stopped at least 2 months before starting the study 8. Antihypertensive treatment prior to initiating the trial; stopped at least 2 months before starting the study 9. Diabetes mellitus (fasting blood glucose \> 126 mg/dL; measurements repeated for confirmation) 10. Renal disease (plasma creatinine levels \> 1.4 mg/dL for women and \> 1.5 mg/dL for men 11. Acute infectious diseases, malignancies, severe liver insufficiency, chronic respiratory insufficiency or associated endocrine diseases 12. Other conditions with special nutritional requirements 13. Having participated in a clinical trial in the last 3 months, or currently participating in a clinical trial 14. Inability to continue in the study 15. History of gastrointestinal disease that can impair the absorption of nutrients 16. Depression syndrome or self-injuring ideation 17. High plasma C-reactive protein and ESR concentrations 18. Immunization in the last 2 months 19. Anemia

Design outcomes

Primary

MeasureTime frameDescription
Changes in the dose-response study with olive oils (FOO250, FOO500 and FOO750) enriched with broad-spectrum phenolic compoundsChanges from baseline (pre-ingestion) in Bioavailability of phenolic compounds at 8h after olive oil intakeBioavailability of phenolic compounds from olive oils in plasma and urine until 8h post olive oil-intake.

Secondary

MeasureTime frameDescription
Changes of bioactivity with olive oild (FOO250, FOO500 and FOO750)enriched with broad-spectrum phenolic compoundsChanges form baseline (pre-ingestion) in endothelial function of phenolic compounds at 6h after olive oilEndothelial function will be measured through the assessment of ischemic reactive hyperemia (IRH), at baseline and at 2h, 4 h and 6 after olive oil intake
Changes in bioactivity of FOO250, FOO500 and FOO750Changes form baseline (pre-ingestion) at 6h or 8h after oral olive oil intake in bioactivityBiomarkers of cardiovascular disease: Oxidative; Lipid profile; Insulin resistance; Inflammation biomarkers; Endothelial dysfunction; Anti-thrombotic activity; Identification and quantification in human plasma and in urine of phenol metabolites

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026