Effect of Probiotics as Supplement to Non-surgical Periodontal Treatment

Status Recruiting

Clinical Trial Summary

The present study is a double-blinded randomized clinical trial with a duration of 12 weeks.

Clinical Trial Description

The present study is a double-blinded randomized clinical trial with a duration of 12 weeks . 60 patients with periodontitis stage 2-3, grade B-C, generalized will be allocated in the test (probiotic) and the control (placebo) group at baseline. The intervention is non-surgical periodontal treatment, which will be applied at baseline and followed for 12 weeks. Clinical measurements and sampling will be performed at baseline, week 6 and week 12. Primary endpoint: Changes in microbial composition. Secondary endpoints: Changes in clinical and immunological parameters ;

Study Design

Related Conditions & MeSH terms

Periodontitis

Clinical Trial Details

NCT number	NCT05518747
Study type	Interventional
Source	University of Copenhagen
Contact
Status	Recruiting
Phase	N/A
Start date	September 1, 2022
Completion date	December 31, 2023

View Details

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