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Oral Pomegranate Extract on the Microbiome and Skin Biophysical Properties

Prospective Randomized Double-Blind Placebo Controlled Study of Oral Pomella on the Microbiome and Skin Biophysical Properties

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04596722
Enrollment
18
Registered
2020-10-22
Start date
2020-11-09
Completion date
2021-03-24
Last updated
2021-04-13

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

Conditions

Human Microbiome

Keywords

gut microbiome, polyphenols, skin, dermatology, pomegranate extract, punicalagins

Brief summary

Pomegranate extract (Pomella) is well known for its antioxidant properties due to its phenolic compounds. It has also been shown to increase the amount of short chain fatty acid producing Lactobacillus and Bifidobacteria genera. Short chain fatty acids are thought to have an anti-inflammatory effect on the sebaceous glands. Previous studies have concluded that pomegranate extract may act as a prebiotic in the body and subsequently increasing the gastrointestinal microbial diversity and by producing short chain fatty acids that may have systemic beneficial effects especially on the skin. Therefore, the aim of this study is to assess how Pomella alters the gut microbiome and the blood level of short chain fatty acids in healthy subjects.

Interventions

DIETARY_SUPPLEMENTPomella

Pomella® Pomegranate Whole Fruit Extract containing 75 mg punicalagin in white/white HPMC size 1 capsules packed in white color HDPE bottle of 30 counts

OTHERPlacebo

White/white HPMC size 1 capsules each containing 97.67% Maltodextrin, 0.10% Tartrazine color, 0.22% Brown Color, 2.01% Aerosil packed in white color HDPE bottle of 30 counts

Sponsors

Verdure Sciences
CollaboratorINDUSTRY
Integrative Skin Science and Research
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
25 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

1. Subjects aged 25-55 2. Must be willing to comply with all protocol requirements 3. Must be willing to have flash photo facial images taken with the imaging systems 4. Males must be willing to shave any facial hair

Exclusion criteria

1. Any systemic or antibiotics (injected or oral) within 6 months of starting study 2. Any topical antibiotic or benzoyl peroxide within 1 month of starting study or any subject unwilling to refrain from washout of topical antibacterial or benzoyl peroxide ingredient. 3. No intake of alcohol or tea throughout the duration of the study. 4. No more than 1 8 oz cup of coffee per week throughout the duration of the study. 5. No more than 1 cup of berries (strawberries, blueberries, raspberries, blackberries, etc.) per week throughout the duration of the study. 6. No intake of pomegranate, or pomegranate-containing drinks throughout the duration of the study. 7. No intake of chocolate (in any form) throughout the duration of the study. 8. No more than 1 cup of fermented dairy products per week throughout the duration of the study. 9. Any oral probiotic or prebiotic supplementation within past 1 month 10. Subjects must have no history of malignancy or cancer or diagnosis of gastrointestinal inflammatory diseases, no history or diagnosis of epilepsy, no history or diagnosis of immunologic or infectious disease (e.g. hepatitis, tuberculosis, HIV or AIDS, lupus, rheumatoid arthritis) 11. Has a condition or is on medication the investigator and/or designee believe could jeopardize the safety of the subject, interfere with the evaluation, or confound the interpretation of the study results 12. Women who have been pregnant in the last three months, are pregnant, preparing to be pregnant or lactating. 13. Is participating in a concurrent clinical research study or has participated in an acne or other facial study at this or any other facility in the past 4 weeks 14. Those with BMI higher than 35 kg/m² 15. Commencement of a new diet (such as the ketogenic diet) or supplements within the 1 month prior to initiating participation, at the discretion of the investigator. 16. Use of medications that alter blood lipids, such as statins and anti-hyperlipidemic medications 17. Is participating in or has participated in a facial study at this or any other facility in the past 4 weeks. Participation in survey-based studies are approved at the discretion of the investigator. 18. Has a skin disease on face that will interfere with image collection and assessment in the opinion of the investigator 19. Refusal to shave or remove facial hair that may interfere with image collection and assessment. 20. Persons unwilling to avoid the following during the 4 weeks prior and during the duration of the study: self-tanning, spa tanning, sun tanning, or artificial tanning. 21. Planned vacation to sunny destination with the intention of sun tanning during the duration of the study. 22. Persons who regularly undergo sauna treatments (dry or wet) or who swim daily. 23. Known allergy or irritation to the supplement or facial products utilized in the study 24. Current tobacco smokers, OR those that have smoked tobacco over the past year, OR a 5 year-pack year history of smoking tobacco 25. Prisoners 26. Adults unable to consent 27. Vegans

Design outcomes

Primary

MeasureTime frameDescription
Shift in Gut Microbiome Diversity4 weeksStool is collected and analyzed for species of bacteria through nucleic acid sequencing.

Secondary

MeasureTime frameDescription
Gut Microbiome Changes- Abundance and Presence of Short Chain Fatty Acid producing Bacteria4 weeksStool is collected and analyzed for species of bacteria through nucleic acid sequencing.
Safety Assessment for GI Distress4 weeksSubjective GI based Questionnaire that will assess for distress (one combined metric that accounts for stooling, gas, and discomfort)
Change in Skin Brightness - Device based4 weeksSkinColorCatch colorimeter RGB range: 25-246 per channel
Change in Sebum Excretion Rate4 weeksDelfin Sebumeter: 0-150 micrograms/cm\^2
Change in the Appearance of Facial Redness and Facial Skin Tone4 weeksSkinColorCatch colorimeter RGB range: 25-246 per channel; BTBP Clarity Mini 3D\_V5 camera
Shift in the Blood Short Chain Fatty Acid Levels4 weeksShort chain fatty acids are measured from a venipuncture
Change in skin brightness - image based4 weeksBTBP Clarity Mini 3D Camera
Change in Transepidermal Water Loss4 weeksDelfin Vapometer 0-300g/m\^2h; Delfin MoisturemeterSC 0-150

Other

MeasureTime frameDescription
Change in Skin Microbiome Diversity4 weeksThe alpha and beta diversity of facial skin microbiome collections will be evaluated

Countries

United States

Outcome results

None listed

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