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Probiotics Effects to Initial Periodontal Treatment

Clinical and Microbiological Evaluation of Probiotics as an Adjunct to Initial Periodontal Treatment in Chronic Periodontitis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05408364
Enrollment
30
Registered
2022-06-07
Start date
2011-04-30
Completion date
2013-04-30
Last updated
2022-06-07

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

Conditions

Chronic Periodontitis

Keywords

bifidobacterium, chronic periodontitis, dental scaling, probiotic, root planing

Brief summary

The aim of this study is to evaluate the clinical and microbiological effects of Bifidobacterium animalis subsp. lactis DN-173010 containing yoghurt as an adjunct to mechanical periodontal treatment.

Detailed description

The aim of this study is to evaluate the clinical and microbiological effects of Bifidobacterium animalis subsp. lactis DN-173010 containing yoghurt as an adjunct to mechanical periodontal treatment. Thirty chronic periodontitis patients were randomized into 2 groups. As adjunctive to MPT, Group 1 consumed 2×108 CFU/day of Bifidobacterium animalis subsp. lactis DN-173010 containing probiotic yoghurt while Group 2 natural yoghurt once daily for 28 days. Subgingival plaque samples were obtained from 2 periodontal sites with probing pocket depth (PPD) of 4≤PPD\<7 mm via paper-points at baseline, 28th day, 3rd month. Samples were cultured to evaluate total viable count (TVC), the proportions of obligate anaerobes (OA) and Bifidobacterium species (B) (TVC%). The full-mouth recorded clinical parameters were plaque index, gingival index, PPD, bleeding on probing, and clinical attachment level.

Interventions

DIETARY_SUPPLEMENTprobiotic or natural yoghurt

Bifidobacterium animalis subsp. lactis DN-173010 containing probiotic yoghurt

PROCEDURESRP

Scalling and root planing

Sponsors

Marmara University
Lead SponsorOTHER

Study design

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

Masking description

Individuals and doctor were blinded to the study groups allocation. Before statistical analysis, the blind study coordinator broke the code to allocate the indivuals to the groups.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* chronic periodontitis patients with radiographically detected horizontal bone loss * the presence of at least 2 teeth with one approximal site with a probing pocket depth (PPD) of 4≤SD\<7 mm (5-7 mm) and a GI of ≥2 mm in each quadrant, * previously untreated periodontitis, systemically healthy

Exclusion criteria

* Systemic diseases * Antibiotics and anti-inflammatory drugs within 3 months before the study * Untreated caries lesions or local retention factors * Allergic reactions to lactose or fermented milk products * Previous probiotic supplements in diet * Smoking * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Probing Depth28 daysProbing depth is defined as the distance from the free gingival margin to the bottom of the periodontal pocket.

Secondary

MeasureTime frameDescription
Gingival Index28 daysEach of the buccal, mesial, lingual and distal surfaces of the gingival tissues is given a score of 0-3. (0 = Normal gingiva. 1 = Mild inflammation - slight change in color, slight edema. No bleeding on probing. 2. Moderate inflammation - redness, edema and glazing. Bleeding on probing. 3. Severe inflammation -marked redness and edema.)
Plaque Index28 daysEach of the four surfaces of the teeth (buccal, lingual, mesial and distal) is given a score from 0-3. (0 = No plaque in the gingival area. 1 = A film of plaque adhering to the free gingival margin and adjacent area of the tooth. The plaque may only be recognized by running a probe across the tooth surface. 2 = Moderate accumulation of soft deposits within the gingival pocket, on the gingival margin and/or adjacent tooth surface, which can be seen by the naked eye. 3 = Abundance of soft matter within the gingival pocket and/or on the gingival margin and adjacent tooth surface. Tendency to spontaneous bleeding.)
Bleeding on probing28 daysBleeding on probing is defined as presence of bleeding from gingival sulcus during the probing of this area via periodontal probe.
Clinical attachment level28 daysThe distance from the cementoenamel junction to the bottom of the periodontal pocket.
microbiological parameters28 daysThe number of obligate anaerobic bacteria and Bifidobacterium anaerobes

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026