NCT07366229

Brief Summary

A growing body of evidence suggests that the development and progression of acne are closely linked to an imbalance in the skin's microbial community. Compared to healthy skin, the composition and function of the microbiota in acne lesions are significantly altered. This microbial imbalance is believed to drive the formation and recurrence of acne through mechanisms such as triggering abnormal inflammatory responses and compromising the skin barrier. An in-depth exploration of the interaction between acne and the skin microbiome not only offers new perspectives for understanding the root causes of the disease but also lays the groundwork for developing novel treatment strategies aimed at modulating the microbiota. Therefore, identifying innovative approaches that integrate acne treatment with the regulation of microbial balance holds significant clinical and social value. Although existing acne treatments have made progress, research focusing on interventions that regulate the local skin microecology through probiotics remains relatively limited. This study aims to explore a new strategy based on skin microecological modulation. We are using a common probiotic-Lactobacillus reuteri-and applying an engineering modification with a special coating formed by zinc sulfate and tannic acid (MPN coating). This modification is intended to enhance the bacterium's survival and colonization on the skin, thereby more effectively regulating the local microbiota and reducing inflammation. This study is a rigorous scientific clinical trial designed as randomized, double-blind, and controlled. Eligible participants will be randomly assigned to one of four groups, receiving either the engineered Lactobacillus reuteri cream, the plain Lactobacillus reuteri cream, a simple moisturizing cream (placebo), or an already-marketed effective cream (tretinoin cream). The treatment will last for 2 weeks, followed by an 8-week observation period. Efficacy and safety will be evaluated through professional assessments. Our goal is to scientifically evaluate the safety and efficacy of this new therapy, hoping to provide a potential new treatment option for individuals with acne and explore new pathways for improving skin health.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
196

participants targeted

Target at P75+ for phase_2

Timeline
2mo left

Started Dec 2025

Shorter than P25 for phase_2

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress71%
Dec 2025Jun 2026

Study Start

First participant enrolled

December 30, 2025

Completed
18 days until next milestone

First Submitted

Initial submission to the registry

January 17, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 26, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 30, 2026

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Expected
Last Updated

January 26, 2026

Status Verified

December 1, 2025

Enrollment Period

3 months

First QC Date

January 17, 2026

Last Update Submit

January 17, 2026

Conditions

Keywords

acneLactobacillus reuteri

Outcome Measures

Primary Outcomes (1)

  • Percentage change in acne count at Week 8 relative to the baseline.

    Facial photographs of patients are taken before treatment and at Weeks 1, 2, 4, and 8 after the initial treatment. Dermatologists count the number of acne lesions from these photographs. The percentage change in acne count at Week 8 relative to the baseline is calculated as: (Acne count at Week 8 - Acne count at baseline) / Acne count at baseline × 100%.

    Facial photographs of the patients will be taken at baseline and at Weeks 1, 2, 4, and 8 after the initial treatment, and the number of acne lesions will be counted by dermatologists.

Secondary Outcomes (3)

  • Percentage change in the number of inflammatory acne lesions at Week 8 relative to the baseline

    Facial photographs of the patients will be taken at baseline and at Weeks 1, 2, 4, and 8 after the initial treatment, and the number of inflammatory acne lesions will be counted by dermatologists.

  • Percentage change in the number of non-inflammatory acne lesions at Week 8 relative to the baseline

    Facial photographs of the patients will be taken at baseline and at Weeks 1, 2, 4, and 8 after the initial treatment, and the number of non-inflammatory acne lesions will be counted by dermatologists.

  • Changes in the relative abundance of Propionibacterium, Lactobacillus, and Staphylococcus in acne-prone skin from baseline to Week 8

    Skin microbiome samples are collected from acne lesions at baseline and at Weeks 1, 2, 4, and 8 after the initial treatment.

Study Arms (4)

Experimental Group

EXPERIMENTAL

Apply the MPN-coated engineered Lactobacillus reuteri cream to acne lesions once daily for 2 weeks.

Biological: MPN-coated engineered Lactobacillus reuteri cream

Positive Control Group

ACTIVE COMPARATOR

Apply the 0.1% tretinoin cream to acne lesions once daily for 2 weeks.

Drug: Tretinoin cream 0.1%

Negative Control Group

PLACEBO COMPARATOR

Apply the petrolatum-glycerin cream to acne lesions once daily for 2 weeks.

Drug: Petrolatum-glycerin cream

Control Group

OTHER

Apply the plain Lactobacillus reuteri cream to acne lesions once daily for 2 weeks.

Biological: Plain Lactobacillus reuteri cream

Interventions

Each night before bedtime, after washing the face, an appropriate amount of MPN-coated engineered Lactobacillus reuteri cream should be applied topically to acne lesions using a sterile cotton swab. The area should not be washed immediately after application. Normal face washing can be resumed the following morning. This regimen should be continued for 2 weeks.

Experimental Group

Each night before bedtime, after washing the face, an appropriate amount of plain Lactobacillus reuteri cream should be applied topically to acne lesions using a sterile cotton swab. The area should not be washed immediately after application. Normal face washing can be resumed the following morning. This regimen should be continued for 2 weeks.

Control Group

Each night before bedtime, after washing the face, an appropriate amount of petrolatum-glycerin cream should be applied topically to acne lesions using a sterile cotton swab. The area should not be washed immediately after application. Normal face washing can be resumed the following morning. This regimen should be continued for 2 weeks.

Negative Control Group

Each night before bedtime, after washing the face, an appropriate amount of 0.1% tretinoin cream should be applied topically to acne lesions using a sterile cotton swab. The area should not be washed immediately after application. Normal face washing can be resumed the following morning. This regimen should be continued for 2 weeks.

Positive Control Group

Eligibility Criteria

Age18 Years - 33 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Subjects must be diagnosed with acne (based on history, clinical manifestation, and dermatoscopy) and classified as Grade I to III per the International Improved Grading System.
  • Subjects must be willing and able to provide written informed consent.
  • Subjects must be 18 to 33 years of age and in generally good health.
  • Subjects must have more than 9 inflammatory lesions.

You may not qualify if:

  • Have used antibiotics within 1 month before the study start.
  • Have used systemic retinoid therapy within 3 months before the study start.
  • Have undergone any other acne treatment within 1 month before the study start.
  • Have any other condition that the investigator considers would make participation unsuitable (e.g., deemed unreliable, non-compliant, or unable to comprehend the study assessments).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shenzhen People's Hospital

Shenzhen, Guangdong, China

Location

MeSH Terms

Conditions

Acne Vulgaris

Condition Hierarchy (Ancestors)

Acneiform EruptionsSkin DiseasesSkin and Connective Tissue DiseasesSebaceous Gland Diseases

Central Study Contacts

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Experimental Group Intervention: Apply the MPN-coated engineered Lactobacillus reuteri cream to acne lesions once daily for 2 weeks. Control Group Intervention: Apply the plain Lactobacillus reuteri cream to acne lesions once daily for 2 weeks. Negative Control Group Intervention: Apply the petrolatum-glycerin cream to acne lesions once daily for 2 weeks. Positive Control Group Intervention: Apply the 0.1% tretinoin cream to acne lesions once daily for 2 weeks.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 17, 2026

First Posted

January 26, 2026

Study Start

December 30, 2025

Primary Completion

March 30, 2026

Study Completion (Estimated)

June 30, 2026

Last Updated

January 26, 2026

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations