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Innovative Biotechnological Production of Antioxidant Products

Innovative Biotechnological Production of Antioxidant Products of Plant Origin From Microbial Factories, and Essential Oils From the Greek Flora, for the Creation of New Quality Health Products and Nutritional Supplements

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05679310
Acronym
Antiox-Plus
Enrollment
12
Registered
2023-01-10
Start date
2022-02-10
Completion date
2022-09-30
Last updated
2023-01-10

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

Conditions

Body Weight, Homocystine; Metabolic Disorder, Inflammation, Oxidative Stress

Brief summary

Several natural compounds have been explored as immune-boosting, antioxidant, and anti-inflammatory dietary supplements. Amongst them, hydroxytyrosol a natural antioxidant found in olive products, and endemic medicinal plants have attracted the scientific's community and industry's interest. The safety and biological activity of a standardised supplement containing 10 mg of hydroxytyrosol synthesized using genetically modified Escherichia coli strains and equal amounts (8.33 μL) of essential oils from oregano vulgaris, sage officinalis and crithmum maritimum in an open-label, single-arm, prospective clinical study were studied. The supplement capsules were given to 12 healthy subjects, aged 26-52, once a day for 8 weeks.

Detailed description

The study was designed to evaluate the safety and biological activity of the supplement Antiox-Plus: one capsule/day, 15 minutes before their main meal which contained 10 mg of HT, synthesised using genetically modified Escherichia coli strains and equal amounts (8.33 μL) of essential oils from Origanum vulgare, Sage officinalis and Crithmum maritimum. The volunteers will consume the supplement for 8 weeks. A follow-up analysis will be performed one month after the end of the supplementation period (12 weeks from the initiation of the study). During this time, the participants will consume a placebo. The volunteers are instructed to maintain their normal dietary habits. The following measurements will be taken: A) Dietary assessment at the beginning of the study (week 0), B) Body composition analysis at the beginning (week 0) and the end of the study (week 8), C) biochemical and laboratory analysis of plasma samples at week 0, 8 and 12. The volunteers will record their food intake for 3 days (including one day of the weekend) and will fulfil a food frequency questionnaire. Analysis of their data will be done by a certified nutritionist. Nutritional assessment will be performed using the Evexis dietary software. The Tanita Dual Frequency Body Composition Monitor Innerscan will be employed to measure weight, muscle mass, muscle quality score, heart rate, body fat (%), physique rating, visceral fat, metabolic age, basal metabolic rate, bone mass, body water (%) and body mass index (BMI) in the morning. Physical activity will be assessed by the Greek version of the short International Physical Activity Questionnaire (IPAQ-short).

Interventions

DIETARY_SUPPLEMENTHydroxytyrosol/Essential oils

A dietary supplement containing 10 mg of hydroxytyrosol, synthesised using genetically modified Escherichia coli strains and equal amounts (8.33 μL) of essential oils from oregano vulgaris, sage officinalis and crithmum maritimum.

Sponsors

University of Ioannina
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* age between 25 and 65 years * the absence of any chronic health conditions * adequate understanding of the study

Exclusion criteria

* the presence of any chronic health conditions (diabetes, hypertension, dyslipidemia) * intake of nutritional supplements over the past 60 days * heavy smokers (≥25 cigarettes/day) * high alcohol use (men \>14 drinks/week, women \>7 drinks/week)

Design outcomes

Primary

MeasureTime frameDescription
Fasting blood glucoseChange from Baseline up to 12 weeksFasting blood glucose (md/dL)
oxLDLChange from Baseline up to 12 weeksoxLDL (mU/mL)
HomocysteineChange from Baseline up to 12 weeksHomocysteine (μmol/L)

Secondary

MeasureTime frameDescription
CatalaseChange from Baseline up to 12 weeksCatalase (units/mL)
GlutathioneChange from Baseline up to 12 weeksGlutathione (mU/mL)
LDL-cholesterolChange from Baseline up to 12 weeksLDL-cholesterol (mg/dL)
HDL-cholesterolChange from Baseline up to 12 weeksHDL-cholesterol (mg/dL)

Other

MeasureTime frameDescription
Total Antioxidant CapacityChange from Baseline up to 12 weeksTotal Antioxidant Capacity (mM a-tocopherol)
MalonaldehydeChange from Baseline up to 12 weeksMalonaldehyde (μΜ)

Countries

Greece

Outcome results

None listed

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