Skip to content

Clinical Effect of Lactobacillus Reuteri in Treatment of Gingivitis

Clinical Effect of Lactobacillus Reuteri in Treatment of Gingivitis. Randomized Clinical Trials

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02801773
Enrollment
20
Registered
2016-06-16
Start date
2016-06-30
Completion date
2016-12-31
Last updated
2016-06-21

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

Conditions

Gingivitis

Keywords

gingivitis, probiotic, non- surgical treatment

Brief summary

The aim of this randomized placebo- controlled clinical trials is to evaluate the effects of Lactobacillus reuteri containing probiotic lozenges as an adjunct to scaling and root planning (SRP). Material and methods: Thirty six gingivitis patients will be recruited and monitored clinically at baseline, 3 and 6 month after therapy. All patients will receive scaling and periodontal treatment and randomly will be assigned over an experimental (SRP + probiotic, N=18) or control (SRP+ placebo, n=18) group. The lozenges will be used once per day during 3 month.

Detailed description

Gingivitis is the most prevalent worldwide periodontal disease, is characterized by inflammation of the tissues surrounding the tooth without causing periodontal attachment loss. Preventive and / or therapeutic measures to facilitate or improve their control are therefore very important, much more if you consider that gingivitis and periodontitis are considered part of an ongoing inflammatory process. Treatment of gingivitis, like that of all periodontal diseases has been based on the implementation of control measures personal and professional plaque. Notwithstanding the foregoing, it has been reported that although mechanical therapy achieved significantly decrease the periodontopathogens, this may be only temporary since bacteria can recolonize the treated niches in the oral cavity. In this context, it has emerged as a new treatment strategy complementary use of probiotics such as Lactobacillus reuteri, which possess anti-bacterial and anti-inflammatory properties. Generally speaking, probiotics would promote health by competitive exclusion of some or positive pathogenic bacteria. Objective: To evaluate the effect of the administration of Lactobacillus reuteri as an adjunct to conventional periodontal therapy in adolescent and young adult patients with gingivitis. Methodology: A randomized double-blind clinical trial to evaluate the effect of probiotic lozenges Lactobacillus rhamnosus as an adjunct to conventional periodontal treatment of patients with gingivitis will be performed. Expected Results: Statistically significant decrease in bleeding and gingival index in the experimental group compared with the control.

Interventions

Gingivitis Treatment (scaling and coronary polish) and one lozenge containing Lactobacillus reuteri per day during 3 months

gingivis treatment (scaling and coronary polish) and and one lozenge containing Placebo (mint lozenge) per day during 3 months

Sponsors

University of Chile
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
17 Years to 28 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of Gingivitis * Gingival index \> 1.5 (\> 10 % of sites examined) * Bleeding index \> 10 % sites surveyed * Probing Depth \< 4 mm * Systemically healthy (except for the presence of gingivitis) * Patients who have not received periodontal treatment before the test and no intake of medicines such antibiotic and/ or anti-inflammatory in the last 3 months prior to the start of the study

Exclusion criteria

* Patient who develop systemic disease during the study * Patient who have to ingest antibiotic/ or anti-inflammatories during the study * If you are a woman becomes pregnant during the study

Design outcomes

Primary

MeasureTime frame
Differences between groups for bleeding on probing changesbaseline, 1, 3 month

Secondary

MeasureTime frame
Differences between groups for gingival indexbaseline, 1, 3 month

Countries

Chile

Contacts

Primary ContactJoel E Bravo Bown, Proffesor
jbravo@odontologia.uchile.cl+5694540294

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026