Evaluation of the modified oral microflora stability using chlorhexidine and probiotic in 6-12 years old childre

Phase 4

• Conditions: Dental carries.; dental carries, arested dental carries, other dental carries,dental carries unspecified; k02, k02.3

• Registration Number: IRCT138902183893N1
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 105

Inclusion Criteria

No systematic disease, receiving no medications, not receving any antibiotics or xilytol-containing chewing gums within 4 week prior to the study
Exclusion criteria: salivary SM count lower than 105CFU/ml

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Salivary Streptococcus mutans counts. Timepoint: at 24-hour, one-week, and five-week intervals after cessation of probiotic. Method of measurement: Saliva sampling and microbial evaluation.

Secondary Outcome Measures

Name	Time	Method
actobacilli counts. Timepoint: at 24-hour, one-week, and five-week intervals after cessation of probiotic. Method of measurement: Saliva sampling and microbial evaluation.