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Effect of a Locally Delivered Probiotic in Periodontitis

S

SVS Institute of Dental Sciences

Status and phase

Completed
Phase 2

Conditions

Chronic Periodontitis

Treatments

Procedure: Control site
Procedure: Study site

Study type

Interventional

Funder types

Other

Identifiers

NCT02645669
SVSIDS/PERIO/2/2014
D139406038 (Other Identifier)

Details and patient eligibility

About

Saccharomyces boulardii is commonly employed as a live non-pathogenic probiotic microbial feed or food supplement. S. boulardii reduces the secretion of key pro inflammatory cytokines and promotes the production of anti-inflammatory cytokines such as IL-10, which is pertinent in the context of pathogenic mechanisms in periodontitis.

Full description

One method of altering the subgingival environment is by using probiotics. Probiotics are live microorganisms, which when administered in adequate amounts, confer a health benefit on the host by passively occupying a niche that may otherwise be colonized by pathogens. This tends to limit a pathogen's ability to bind to tissue surfaces and to produce virulence factors.8 In the past few years, probiotics have been investigated for periodontal health. Studies have shown that certain gut bacteria can exert beneficial effects in the oral cavity by inhibiting pathogenic species. Teughels et al., in a study showed that application of beneficial oral bacteria subgingivally after scaling and root planing led to a more host compatible subgingival microbiota which may also effect the promotion of a beneficial host response.10 Studies have revealed that probiotic Lactobacillus strains (L. reuteri, L salivarius, L. casei, L. acidophilus) were useful in reducing gingival inflammation and the number of black-pigmented rods, including Porphyromonas gingivalis, in the saliva and subgingival plaque. Streptococcus sanguinis & S. uberis were found to inhibit the growth of periodontopathogens & a strong negative between Aggregatibacter actinomycetemcomitans and S. sanguinis. Weissella cibaria isolates in the form of probiotic rinse possess the ability to inhibit biofilm formation, both in vitro and in vivo.

Enrollment

30 patients

Sex

All

Ages

25 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subjects having at least one pocket ≥5 mm in each quadrant were included in the study.

Exclusion criteria

  • Medically compromised patients and patients having received any form of surgical or non-surgical therapy in the 6 month period leading to the study were not included.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups, including a placebo group

Study site
Experimental group
Description:
Scaling and Root planing (SRP) was followed by placement of S boulardii-FOS mixture
Treatment:
Procedure: Study site
Control site
Placebo Comparator group
Description:
Only Scaling and Root planing (SRP) was performed
Treatment:
Procedure: Control site

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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