The Relationship Between Microbioma Balance and Acne Vulgaris as a New Acne Treatment

ConditionAcne Vulgaris
Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age13-45
SponsorUniversitas Padjadjaran

About this trial

Background: Acne vulgaris is a chronic inflammatory condition primarily caused by Cutibacterium acnes, which disrupts skin homeostasis, thereby triggering immune responses and sebum metabolism. Dysbiosis is an imbalances in the skin and gut microbiota identified as a significant factor contributing to acne progression. Standard therapy often rely on antibiotics, but the long-term use has increased antibiotic resistance, including in Indonesia. Consequently, alternative methods, such as probiotics and mesenchymal stromal cell (MSC) secretomes are gaining attention for immunomodulatory and regenerative properties. These novel therapies have shown promising results in modulating the skin and gut microbiota while reducing inflammation.

Study Design: A phase 2 double-blind randomized controlled trial was adopted using a parallel group design with four arms, namely: (1) standard therapy with oral probiotics and topical secretome (placebo), (2) standard therapy with oral probiotics (placebo) and topical secretome, (3) standard therapy with oral probiotics and topical secretome, and (4) standard therapy with oral probiotics (placebo) and topical secretome (placebo). Sixty-four mild to moderate acne vulgaris patients were randomly allocated to these groups. Interventions were administered over a period of 8 weeks, with outcomes measured at baseline and post-therapy. This study was conducted at Dermatology and Venereology Department of Bali Mandara General Hospital (RSBM). The primary outcome is the reduction of comedones and inflammatory lesions, assessed using the Yolov8 method. Secondary outcomes include gut and skin health parameters, such as tryptophan metabolites, collagen, pH, moisture, sebum levels, and IL-6, to explore the relationship between microbiome balance, skin condition, and inflammation in acne.

Discussion: In the context of increasing antibiotic resistance in Indonesia, where therapies often fail to produce sustainable clinical outcomes, this study showed the potential of combining probiotics and MSC secretomes as adjunctive therapies for acne vulgaris. Probiotics restored gut and skin microbiota balance, while MSC secretomes promoted immune modulation and tissue repair. The results of this study paved the way for innovative, non-antibiotic methods for acne management, addressing the need for sustainable and effective therapies amidst growing concerns over dysbiosis and antibiotic resistance.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

individuals aged 13 to 45 years

diagnosed with acne vulgaris by a certified dermatologist, presenting with mild to moderate facial acne based on the lesion count criteria by Lehman et al. Mild acne is defined as having fewer than 20 comedones or fewer than 15 papular/pustular lesions, while moderate acne is characterized by 20-100 comedones and 20-50 papular/pustular lesions.

must have experienced recurring new acne lesions in the past 6 months

must be willing to comply with all protocol requirements

Disqualifiers

pregnant patients

subjects who have undergone hormonal acne treatment within six months prior to the study

subjects who have taken oral isotretinoin within one month prior to the study.

simultaneous participation in a different study conducted by an external research institution at the same testing site.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Standard therapy

    Drug

    The standard therapy for participants included a structured skincare regimen. A face wash was used once daily before bedtime to cleanse the skin. In the morning, a non-comedogenic sunscreen and a moisturizer were applied to protect and hydrate the skin. Additionally, a night cream containing clindamycin and tretinoin was applied once daily at night, specifically on acne-affected areas, to target inflammation and promote skin renewal.

  • HEXBIO

    Dietary supplement

    The oral probiotics given are Hexbio®, an oral probiotic containing multiple beneficial bacterial strains, including Lactobacillus acidophilus BCMC® 12130, Lactobacillus casei BCMC® 12313, Lactobacillus lactis BCMC® 12451, Bifidobacterium bifidum BCMC®02290, Bifidobacterium longum BCMC® 02120, and Bifidobacterium infantis BCMC®02129. This probiotic was administered in granule form and swallowed directly. Participants consumed the probiotic twice daily, after breakfast and dinner, for eight weeks to support gut microbiome balance and potential skin health benefits.

  • Secretome

    Biological/Vaccine

    The topical secretome used is a hydrogel-based serum containing secretome components, including cytokines, growth factors, exosomes, microvesicles, and cell differentiation factors. The serum is formulated with a hydrogel base consisting of xanthan gum, sclerotium gum, 1% alginate, 2% glycerin, 1% caprylyl glycol, and 96% aqua. It is applied after cleansing the face with a facial cleanser, twice daily, in the morning and evening, for eight weeks

Treatment groups

64 Participants
are divided into 4 treatment groups
Group A: Group 1Experimental treatment 2 interventions
Group B: Group 2Experimental treatment 2 interventions
Group C: Group 3Experimental treatment 3 interventions
Group D: Group 4Placebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Reduction of comedones and inflammatory lesions

The primary outcome measured in this study is the reduction in the number of comedones and/or inflammatory lesions (papules/pustules). This is assessed using the Yolov8 machine learning detection method, which enables accurate and objective quantification of comedones and lesions while also determining the severity of acne

Time frame
From enrollment to the end of treatment at 8 weeks

Secondary outcomes

1

Tryptophan metabolites

In the gut, tryptophan metabolites are measured using the ELISA method to assess the abundance of probiotic bacteria, specifically lactic acid bacteria such as Lactobacillus and Bifidobacterium

Time frame
From enrollment to the end of treatment at 8 weeks
2

Inflammatory Response

Inflammatory responses are assessed by measuring serum IL-6 levels, which serve as an indicator of systemic inflammation

Time frame
From enrollment to the end of treatment at 8 weeks
3

Collagen Measurement

collagen measurement use skin Elastometer

Time frame
From enrollment to the end of treatment at 8 weeks
4

Moisture content

Moisture content use skin hydrometer

Time frame
From enrollment to the end of treatment at 8 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Universitas Padjadjaran

Lead sponsor

PT. Prodia Stem Cell Indonesia

Collaborator

B-Crobes Laboratory (M) Sdn Bhd

Collaborator

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