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Study of Skin Balancing Gel Cream Safety and Influence of Skin Microbiome on Acne Prone Skin

Open-label, Prospective Study of Skin Balancing Gel Cream Safety and Influence of Skin Microbiome on Acne Prone Skin

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05941065
Enrollment
30
Registered
2023-07-12
Start date
2023-09-01
Completion date
2024-04-30
Last updated
2023-10-10

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

Conditions

Acne, Skin Microboime

Keywords

Skin, Microbiome

Brief summary

The purpose of this study is to assess the safety of the skin balancing gel cream and examine the effects it has on the skin microbiome of individuals with non-cystic acne prone skin.

Detailed description

Acne, a chronic inflammatory condition, is estimated to affect greater than 85% of the population at some point. It is considered a common skin condition characterized by pimples and occurs when follicles are clogged leading to the formation of acne lesions. In this study, we want to evaluate the impact the skin balancing gel cream has on the skin microbiome on individuals who have mild to moderate non-cystic acne. We will be assessing the changes it has on specific microbiota (Cutibacterium acnes for example) and whether it is tolerated well on acne prone skin.

Interventions

OTHERBalancing gel cream

Skin balancing gel cream will be applied onto clean skin morning and night

Sponsors

Burt's Bees Inc.
CollaboratorINDUSTRY
Integrative Skin Science and Research
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Males and females between the ages of 18 years of age until 35 years of age * Males must be willing to shave facial hair * The presence of mild to moderate non-cystic acne based on investigator global assessment

Exclusion criteria

* Individuals who are pregnant or breastfeeding. * Prisoners. * Adults unable to consent. * The presence of severe acne or cysts as noted by the investigator. * Those who are unwilling to discontinue topical antibiotics, topical salicylic acid containing products and topical benzoyl peroxide containing products for two weeks to meet the washout criteria prior to enrolling. * Those who are unwilling to discontinue all facial topical products except the cleanser and the product provided in the study. * Individuals who have been on an oral antibiotic for acne within the previous 1 month. * Individuals who have changed any of their hormonal based contraception within 3. months prior to joining the study. * Current tobacco smoker or a tobacco smoking history of greater than 10 pack-years.

Design outcomes

Primary

MeasureTime frameDescription
C. acnes relative abundance6 weeksShift in the C. acnes relative abundance based on skin microbiome swab collection and sequencing

Secondary

MeasureTime frameDescription
Functional gene based predictive analysis of skin inflammation related genes6 weeksFunctional gene analysis for skin inflammation related genes from whole genome sequencing of facial skin microbiome
Sebum excretion rate6 weeksMeasure of skin sebum via sebumeter
Tolerability Assessment Questionnaire6 weeksA 6 question survey based on the self-assessment about the tolerability of the topical skin product such as itching, burning, and stinging. The scale ranges from 0-3 with 0 being the best outcome possible and with 3 being the worst. 0 as none, 1 as mild, 2 as moderate, or 3 as severe.
Total lesion count6 weeksSafety endpoint to count inflammatory and non-inflammatory lesions to ensure that there is not a flare in the acne

Countries

United States

Contacts

Primary ContactNhi Nguyen
research@integrativeskinresearch.com916-750-2463

Outcome results

None listed

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