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Clinical Trial Summary

The aim of the study is to assess if probiotic supplementation can be effective in reducing periodontal clinical parameters in a 6-month study on pregnant patients.


Clinical Trial Description

The aim of the study is to assess if probiotic supplementation can be effective in reducing periodontal clinical parameters in a 6-month study on pregnant patients. Patients' enrollment will be conducted according to inclusion criteria. At the first visit, periodontal parameters will be recorded: Plaque Index (PI), recession (R) Bleeding on Probing (BoP), modified Marginal Gingival Index (mMGI), Papillary Marginal Gingival (PMGI), Plaque Control Record ( PCR %), Approximal Plaque Index (API), Clinical Attachment loss (CAL) and Probing Pocket Depth (PPD). Professional debridement will be conducted with piezoelectric instrumentation and air-flow administration with glycine powders. Subsequently, patients will be randomly divided into two groups: - the Probiotic group, in which patients will undergo daily probiotic supplementation in addition to the standard treatment - the Control group, in which patients will undergo standard treatment Professional debridement will be repeated every 3 months. Periodontal index evaluation will be conducted at the baseline (T0), after 1 month (T1), after 3 months (T2), and after 6 months (T3). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06308497
Study type Interventional
Source University of Pavia
Contact
Status Enrolling by invitation
Phase N/A
Start date March 10, 2024
Completion date October 20, 2024

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