- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05756842
Honey Consumption, Oxidative Stress and Health
The Effect of a Honey-based Gel Supplement From the Wider Area of Pindos on Human Health and Oxidative Stress Biomarkers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Introduction: Honey contains about 200 compounds such as sugars, proteins, vitamins, water, free amino acids, enzymes, minerals, and many phytochemicals. Due to its composition, enriched with many bioactive ingredients, several studies have established its antimicrobial, antiviral, anticancer, antidiabetic and antioxidant properties. This multilayer activity of honey has been proposed for the protection against pathologies interrelated with the cardiovascular, nervous, respiratory, and gastrointestinal system.
Purpose: This study aims to investigate the effects of a novel natural honey-based gel consumption on oxidative stress biomarkers, blood chemistry and physiological characteristics in healthy individuals.
Methodology: A total of 20 healthy men and women will participate in the study. Participants will give their informed consent after they will be informed about the purposes, procedures, risks and benefits associated with the study. Participants will consume 70 g/day of the honey-based gel, distributed in 2 equal doses (in the morning and evening) for 14 days. At baseline and post-intervention, volunteers will be assessed for their physiological profile and will provide a resting blood sample for the assessment of oxidative stress and blood chemistry biomarkers as well as their physiological profile. Participants will be asked to record their diet for 3 days prior to the study and they will be asked to follow the same dietary pattern for 3 days before the post-intervention assessments.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Thessaly
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Trikala, Thessaly, Greece, 42150
- Exercise Biochemistry, Physiology and Nutrition Laboratory, Department of Physical Education and Sport Science, University of Thessaly
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy Individuals aged 18-65 years
- Non-smokers
Exclusion Criteria:
- Musculoskeletal injury
- Dietary supplements
- Medication
- Allergy in bee pollen
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Honey-based gel consumption
A honey-based gel will be administered to participants in this arm.
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70 g/day of a honey-based gel divided into 2 equal doses of 35 gr (in the morning and evening) for a total duration of 14 days
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in glutathione concentration of erythrocytes
Time Frame: Change from baseline to 14 days
|
Glutathione concentration will be analyzed in erythrocytes by spectrophotometry
|
Change from baseline to 14 days
|
|
Change in catalase enzyme activity of erythrocytes
Time Frame: Change from baseline to 14 days
|
Catalase enzyme activity will be analyzed in erythrocytes by spectrophotometry
|
Change from baseline to 14 days
|
|
Change in total antioxidant capacity of plasma
Time Frame: Change from baseline to 14 days
|
Total antioxidant capacity will be analyzed in plasma by spectrophotometry
|
Change from baseline to 14 days
|
|
Change in thiobarbituric acid reactive substances of plasma
Time Frame: Change from baseline to 14 days
|
Thiobarbituric acid reactive substances will be analyzed in plasma by spectrophotometry
|
Change from baseline to 14 days
|
|
Change in protein carbonyls of plasma
Time Frame: Change from baseline to 14 days
|
Protein Carbonyls will be analyzed in plasma by spectrophotometry
|
Change from baseline to 14 days
|
|
Change in body weight
Time Frame: Change from baseline to 14 days
|
Body weight will be measured using a digital scale
|
Change from baseline to 14 days
|
|
Change in body fat
Time Frame: Change from baseline to 14 days
|
Body fat will be measured by bioelectrical impedance analysis
|
Change from baseline to 14 days
|
|
Change in resting heart rate
Time Frame: Change from baseline to 14 days
|
Resting heart rate will be measured using a heart rate sensor
|
Change from baseline to 14 days
|
|
Change in diastolic and systolic blood pressure
Time Frame: Change from baseline to 14 days
|
Diastolic and systolic blood pressure will be measured using a manual sphygmomanometer
|
Change from baseline to 14 days
|
|
Change in waist and hip circumference
Time Frame: Change from baseline to 14 days
|
Waist and hip circumference will be assessed using a tape measure
|
Change from baseline to 14 days
|
|
Change in complete blood count
Time Frame: Change from baseline to 14 days
|
White blood cells, lymphocytes, monocytes, granulocytes, red blood cells and platelets will be analyzed in whole blood
|
Change from baseline to 14 days
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Athanasios Z. Jamurtas, Professor, University of Thessaly
Publications and helpful links
General Publications
- Schramm DD, Karim M, Schrader HR, Holt RR, Cardetti M, Keen CL. Honey with high levels of antioxidants can provide protection to healthy human subjects. J Agric Food Chem. 2003 Mar 12;51(6):1732-5. doi: 10.1021/jf025928k.
- Mohd Kamal DA, Ibrahim SF, Kamal H, Kashim MIAM, Mokhtar MH. Physicochemical and Medicinal Properties of Tualang, Gelam and Kelulut Honeys: A Comprehensive Review. Nutrients. 2021 Jan 10;13(1):197. doi: 10.3390/nu13010197.
- Escuredo O, Miguez M, Fernandez-Gonzalez M, Carmen Seijo M. Nutritional value and antioxidant activity of honeys produced in a European Atlantic area. Food Chem. 2013 Jun 1;138(2-3):851-6. doi: 10.1016/j.foodchem.2012.11.015. Epub 2012 Nov 17.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- UTH-HoneyGel
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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