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Microbiological Modulation Of The Oral-Gut Axis After Treatment With Or Without Systemic Use Of Probiotics In Patients With Periodontitis: A Randomized Controlled Clinical Study.

Acronym [*] Required if One Exists. It Will be Included in Parentheses at the End of the Brief Title.

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07792902
Enrollment
40
Registered
2026-08-28
Start date
2026-06-25
Completion date
2026-07-15
Last updated
2026-08-28

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

Conditions

Periodontitis, Periodontitis Stage IV

Keywords

Periodontal Diseases, Gastrointestinal Microbiome, Probiotics, Bifidobacterium animalis, Periodontitis

Brief summary

This study aims to evaluate whether the oral administration of probiotics, in combination with conventional periodontal treatment (deep cleaning of the tooth root surfaces), can improve oral health and influence the relationship between oral and gut bacteria in individuals with periodontitis. The study will include adults aged 30 years or older diagnosed with advanced periodontitis and receiving treatment at the School of Dentistry of Ribeirão Preto, University of São Paulo (FORP/USP). Individuals with systemic diseases that may interfere with the study outcomes, pregnant or breastfeeding women, smokers, recent former smokers, or individuals who have used antibiotics, probiotics, or certain medications within the previous six months will not be eligible to participate. Participants will be randomly assigned to two groups: one group will receive conventional periodontal treatment alone, while the other will receive the same treatment combined with probiotic supplementation. Before and after treatment, periodontal health will be assessed, including the presence of dental plaque, bleeding, periodontal pocket depth, and clinical attachment levels. Inflammatory substances present in gingival fluid will also be analyzed to evaluate the response to treatment. The findings of this study are expected to help clarify whether probiotics used as an adjunct to periodontal treatment can reduce inflammation and promote a more balanced relationship between oral and gut microorganisms, thereby contributing to improved periodontal health.

Detailed description

Periodontitis is a chronic inflammatory disease of multifactorial origin, characterized by the destruction of the tooth-supporting tissues as a result of the interaction between a dysbiotic biofilm and the host immunoinflammatory response. Recent evidence suggests that the oral microbiota may influence the gut microbiota through the oral-gut axis, contributing to local and systemic alterations. In this context, the use of probiotics as an adjunctive therapy to conventional periodontal treatment may favor the restoration of microbial balance and reduce inflammation. The aim of this study is to evaluate the impact of systemic probiotic therapy, used as an adjunct to scaling and root planing (SRP), on the microbiological modulation of the oral-gut axis in patients with periodontitis. In addition, the effects of the intervention on periodontal clinical parameters, the immunoinflammatory profile, and the composition of the oral and gut microbiota will be investigated. This randomized, placebo-controlled clinical trial will include 40 systemically healthy participants aged 30 years or older, diagnosed with generalized Stage III or IV, Grade B/C periodontitis, recruited at the School of Dentistry of Ribeirão Preto, University of São Paulo (FORP/USP). Participants will be randomly allocated into two groups: one group will receive scaling and root planing associated with the probiotic Bifidobacterium animalis subsp. lactis HN019, whereas the other group will receive the same periodontal treatment associated with placebo. The probiotic or placebo will be administered orally at a dose of one capsule per day for 30 days. Periodontal clinical parameters will be recorded, including plaque index, bleeding index, probing depth, bleeding on probing, and clinical attachment level. The immunoinflammatory profile will be evaluated by quantifying CCL19, IL-6, TNF-α, IL-1β, and IL-17 in gingival crevicular fluid using multiplex assays (Luminex). To investigate modulation of the oral-gut axis, subgingival biofilm and fecal samples will be collected before and after the intervention for analysis of the oral and gut microbiota. The results will allow us to determine whether the systemic administration of Bifidobacterium animalis subsp. lactis HN019 enhances the effects of non-surgical periodontal therapy, promoting clinical, immunological, and microbiological improvements compared with placebo.

Interventions

DIETARY_SUPPLEMENTProbiotics Bifidobacterium animalis subsp. lactis HN019

The probiotic group will receive a dietary supplement manufactured by Aché Pharmaceuticals containing the strain Bifidobacterium animalis subsp. lactis HN019, while the control group will receive a placebo.

Sponsors

University of Sao Paulo
Lead SponsorOTHER

Study design

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

Intervention model description

Eligible participants will be randomly allocated to two parallel groups in a 1:1 ratio. Both groups will receive scaling and root planing as conventional periodontal treatment. In addition, the experimental group will receive one daily capsule containing the probiotic Bifidobacterium animalis subsp. lactis HN019 for 30 days, while the control group will receive a placebo capsule with the same appearance and mode of administration. Participants will be followed for 90 days to evaluate clinical, immunological, and microbiological outcomes.

Eligibility

Sex/Gender
ALL
Age
30 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Systemically healthy individuals; * Age of 30 years or older; * Both genders; * At least 15 teeth, excluding third molars and teeth indicated for extraction * At least 30% of the teeth presenting probing depth (PD) and clinical attachment loss (CAL) greater than or equal to 5 mm; * Individuals diagnosed with generalized Stage III or IV, Grade B or C periodontitis; * Presence of at least 8 teeth with at least one non-contiguous interproximal site presenting probing depth (PD) and clinical attachment level (CAL) greater than or equal to 5 mm.

Exclusion criteria

* Current smokers or former smokers who quit within the past 5 years; * Pregnant or breastfeeding women; * History of periodontal treatment within the previous 6 months; * Continuous use of oral antiseptics, systemic antibiotics, corticosteroids, nonsteroidal anti-inflammatory drugs, immunosuppressive agents, estrogen, selective estrogen receptor modulators, or medications that may affect bone metabolism (such as alendronate, calcitonin, and others) within the previous 6 months; * Presence of systemic conditions that may alter the host response to periodontal treatment (such as diabetes, human papillomavirus infection, or Down syndrome) or that require antibiotic prophylaxis before dental treatment (such as mitral valve prolapse); * Use of probiotics within the previous 6 months.

Design outcomes

Primary

MeasureTime frameDescription
Change in clinical periodontal parameters - Plaque index (PI)Baseline and 90 days after periodontal treatment.Changes in clinical periodontal parameters including plaque index (PI) will be compared between the probiotic and placebo groups to evaluate the effect of adjunctive systemic probiotic therapy following scaling and root planing.
Change in clinical periodontal parameters - Bleeding on Probing (BOP)Baseline and 90 days after periodontal treatment.Changes in clinical periodontal parameters including bleeding on probing (POB) will be compared between the probiotic and placebo groups to evaluate the effect of adjunctive systemic probiotic therapy following scaling and root planning.
Change in clinical periodontal parameters - Clinical Attachment Level (CAL)Baseline and 90 days after periodontal treatment.Changes in clinical periodontal parameters including Clinical Attachment Level (CAL) will be compared between the probiotic and placebo groups to evaluate the effect of adjunctive systemic probiotic therapy following scaling and root planning.

Secondary

MeasureTime frameDescription
Change in immunoinflammatory biomarkers in gingival crevicular fluidBaseline and 90 days after periodontal treatment.Changes in the concentrations of inflammatory and immunological biomarkers, including IL-6, TNF-α, IFN-γ, IL-10, IL-1β, and IL-8, measured in gingival crevicular fluid by Luminex immunoassays, will be compared between the probiotic and placebo groups to evaluate the influence of adjunctive systemic probiotic therapy on the host inflammatory response.

Countries

Brazil

Contacts

PRINCIPAL_INVESTIGATORRenata P Aguiar, DDS, Spec

University of Sao Paulo

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 29, 2026