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The Effect of Pomegranate on Aging and Inflammation of the Skin (PomSkin)

Primary Purpose

Skin Photoaging, Inflammation and Skin Pathogenic Bacteria

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pomegranate Extract
Pomegranate Juice
Placebo
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Skin Photoaging, Inflammation and Skin Pathogenic Bacteria

Eligibility Criteria

30 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Age 30-45 years or older, female and any racial/ethnic group
  2. Subjects must understand and sign the informed consent prior to participation
  3. Subjects must be in generally good health
  4. Subjects must be able and willing to comply with the requirements of the protocol.

Exclusion Criteria:

  1. Oral or topical retinoid use within twelve months of entry into the study
  2. Non-compliant subjects
  3. Taking any antibiotics or other medication or dietary supplements regularly
  4. Subjects with a significant medical history or concurrent condition that the investigator(s) feel is not safe for the study
  5. Subjects who cannot avoid excessive exposure to either natural or artificial sunlight.
  6. Allergic to pomegranate products

Sites / Locations

  • UCLA Center for Human Nutrition

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Pomegranate Extract

Pomegranate Juice

Placebo

Arm Description

15 healthy subjects, ages 30-45 years who meet all the eligibility criteria in the screening phase of the study will be assigned to the Pomx arm of the study to evaluate the clinical efficacy of pomegranate extract on skin inflammation and aging. Subjects will be asked to take Pomx 1/day for 12 weeks.

15 healthy subjects, ages 30-45 years who meet all the eligibility criteria in the screening phase of the study will be assigned to the Pomx arm of the study to evaluate the clinical efficacy of pomegranate juice on skin inflammation and aging. Subjects will be asked to take Pomx 1/day for 12 weeks.

15 healthy subjects, ages 30-45 years who meet all the eligibility criteria in the screening phase of the study will be assigned to the Pomx arm of the study to evaluate the clinical efficacy of placebo on skin inflammation and aging. Subjects will be asked to take Pomx 1/day for 12 weeks.

Outcomes

Primary Outcome Measures

Change in inflammatory markers between pomegranate extract and pomegranate juice versus placebo.
Utilization of a two-sample t-test to compare the change in between the three groups

Secondary Outcome Measures

Linear mixed effects models to evaluate effect of treatment of time trends and demographic covariates
Correlation between outcomes measures (e.g. between acne lesion count and skin microbiota) with mixed effects models

Full Information

First Posted
September 26, 2014
Last Updated
February 27, 2017
Sponsor
University of California, Los Angeles
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1. Study Identification

Unique Protocol Identification Number
NCT02258776
Brief Title
The Effect of Pomegranate on Aging and Inflammation of the Skin
Acronym
PomSkin
Official Title
Clinical Trial to Determine the Efficacy of Pomegranate for Skin Inflammation and Aging
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
October 2015 (undefined)
Primary Completion Date
February 27, 2017 (Actual)
Study Completion Date
February 27, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine the efficacy of pomegranate extract and pomegranate juice on skin inflammation and aging. The information gained from this study may lead to the development of a pomegranate product that can decrease the effects of aging, inflammation and harmful bacteria on the skin. In this study, two pomegranate products (extract and juice) will be compared with a placebo, a study product that looks like pomegranate extract, but contains no active ingredients.
Detailed Description
Pomegranate (Punica granatum L.) is grown commercially in the Near East, India, Spain, Israel and the United States (California) where it is of significant economic importance1. Pomegranate fruits and products, including juice, tea, wine and extracts are widely consumed and recognized for their health benefits. Pomegranate (Punica granatum L.) fruit possesses strong antioxidant, anti-inflammatory and antiproliferative properties. In recent years, most health advantages of pomegranate have been attributed to the presence of ellagitannins, mainly punicalagins and ellagic acid. Punicalagin is unique to pomegranate and is part of a family of ellagitannins. The ellagitannins are hydrolyzed to ellagic acid in the gut, and further metabolized by the colon microflora to form urolith A and B. Investigations using pure bacterial cultures have shown that pomegranate by-products and punicalagins significantly inhibited the growth of pathogenic Escherichia coli, Pseudomonas aeruginosa, clostridia and Staphylococcus aureus. Oral feeding of pomegranate fruit extract to mice afforded protection to mouse skin against the adverse effects of ultraviolet-B (UVB) radiation by modulating UVB-induced signaling pathways.5 Hydroalcoholic extract based-ointment from pomegranate was reported improving wound healing in vivo. Pomegranate ellagitannins have been demonstrated to have antimicrobial activity. Punicalagin is unique to pomegranate and is part of a family of ellagitannins. The ellagitannins are hydrolyzed to ellagic acid in the gut, and further metabolized by the colon microflora to form urolith A and B. Investigations using pure bacterial cultures have shown that pomegranate by-products and punicalagins significantly inhibited the growth of pathogenic Escherichia coli, Pseudomonas aeruginosa, clostridia and Staphylococcus aureus. Pomegranate Extract (POMx) is made from pomegranate fruit as a byproduct of pomegranate juice (PJ) production. A second pressing of the fruit liberates a complex mixture of hydrolysable polyphenolic compounds normally ingested with pomegranate juice, and these are purified by spray drying. POMx powder is encapsulated for oral administration, with each capsule containing 1,000 mg of pomegranate polyphenols. The present study will determine whether a pomegranate product (POMx or PJ) can decrease skin photoaging, inflammation and skin pathogenic bacteria.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Skin Photoaging, Inflammation and Skin Pathogenic Bacteria

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pomegranate Extract
Arm Type
Active Comparator
Arm Description
15 healthy subjects, ages 30-45 years who meet all the eligibility criteria in the screening phase of the study will be assigned to the Pomx arm of the study to evaluate the clinical efficacy of pomegranate extract on skin inflammation and aging. Subjects will be asked to take Pomx 1/day for 12 weeks.
Arm Title
Pomegranate Juice
Arm Type
Active Comparator
Arm Description
15 healthy subjects, ages 30-45 years who meet all the eligibility criteria in the screening phase of the study will be assigned to the Pomx arm of the study to evaluate the clinical efficacy of pomegranate juice on skin inflammation and aging. Subjects will be asked to take Pomx 1/day for 12 weeks.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
15 healthy subjects, ages 30-45 years who meet all the eligibility criteria in the screening phase of the study will be assigned to the Pomx arm of the study to evaluate the clinical efficacy of placebo on skin inflammation and aging. Subjects will be asked to take Pomx 1/day for 12 weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
Pomegranate Extract
Intervention Description
Pomegranate extract 1000mg will be taken 1/day for 12 weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
Pomegranate Juice
Intervention Description
Pomegranate juice 8oz will be consumed 1/day for 12 weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo will be taken 1/day for 12 weeks.
Primary Outcome Measure Information:
Title
Change in inflammatory markers between pomegranate extract and pomegranate juice versus placebo.
Description
Utilization of a two-sample t-test to compare the change in between the three groups
Time Frame
Baseline and 12 weeks
Secondary Outcome Measure Information:
Title
Linear mixed effects models to evaluate effect of treatment of time trends and demographic covariates
Description
Correlation between outcomes measures (e.g. between acne lesion count and skin microbiota) with mixed effects models
Time Frame
Baseline and 12 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 30-45 years or older, female and any racial/ethnic group Subjects must understand and sign the informed consent prior to participation Subjects must be in generally good health Subjects must be able and willing to comply with the requirements of the protocol. Exclusion Criteria: Oral or topical retinoid use within twelve months of entry into the study Non-compliant subjects Taking any antibiotics or other medication or dietary supplements regularly Subjects with a significant medical history or concurrent condition that the investigator(s) feel is not safe for the study Subjects who cannot avoid excessive exposure to either natural or artificial sunlight. Allergic to pomegranate products
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhaoping Li, M.D., Ph.D.
Organizational Affiliation
UCLA Department of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCLA Center for Human Nutrition
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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The Effect of Pomegranate on Aging and Inflammation of the Skin

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