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The Effect of Probiotics on Gingivitis

I

I.M. Sechenov First Moscow State Medical University

Status

Completed

Conditions

Gingivitis; Chronic

Treatments

Dietary Supplement: Dentoblis
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT05727436
18081213

Details and patient eligibility

About

The aim of the study is to assess the effect of oral probiotics containing Streptococcus salivarius M18 on gingivitis and oral hygiene in young adults.

Full description

This will be a double-blind, randomized, placebo-controlled two-arm parallel-group study of the effect of oral probiotics containing Streptococcus salivarius M18 on gingivitis and oral hygiene. The groups will include young adults with gingivitis diagnosed clinically. To assess the effect of oral probiotics, the following parameters will be used: gingival index, GI; gingival bleeding index, GBI and oral hygiene level (the Turesky Modification of the Quigley-Hein Plaque Index, TMQHPI).

Enrollment

61 patients

Sex

All

Ages

18 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged between 18-25 years
  • Permanent bite;
  • Presence of more than 20 teeth;
  • Absence of systemic and chronic diseases;
  • The diagnosis of gingivitis stated clinically.

Exclusion criteria

  • Presence of mild, moderate or severe chronic periodontitis;
  • Refusal to sign informed consent;
  • Taking supplements and medication containing probiotics or prebiotics 1 months before the study;
  • Taking antibiotics (within 3 months before the study);
  • Allergy to the components of the drugs used in the study;
  • Presence of immunodeficiency, taking immunosuppressants.
  • Use of other hygiene products, immunostimulants and antibacterials, probiotics, prebiotics during the study;
  • Refusal to take a given medication;
  • Failure to attend check-ups.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

61 participants in 2 patient groups, including a placebo group

Group 1 - probiotic
Experimental group
Description:
Experimental: Group 1 - probiotic The use of Streptococcus salivarius M18 containing tablets ("Dentoblis", registration number: AM.01.06.01.003.R.000061.07.20; 15.07.2020, MEDICO DOMUS, d.d.o.; 18116, Nis, Serbia)) once a day for 4 weeks (before bedtime after evening brushing). Ingredients: basic active ingredients - Streptococcus salivarius M18 (≥5×108 CFU in 1 tablet), Vitamin D (320 IU (8 mcg) in 1 tablet); excipients - isomalt (sweetener), magnesium stearate (vegetable), mint flavoring.
Treatment:
Dietary Supplement: Dentoblis
Group 2 - placebo
Placebo Comparator group
Description:
The use of placebo tablets once a day for 4 weeks (before bedtime after evening brushing). Ingredients: isomalt (sweetener), magnesium stearate (vegetable), mint flavoring.
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

1

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Central trial contact

Ksenia Babina, PhD; Dilara Salikhova

Data sourced from clinicaltrials.gov

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