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NCT07069166Completed

Para-Probiotic Oral Care in Periodontal Patients With Type 2 Diabetes

Evaluation of Para-Probiotic Toothpaste and Mouthwash on Periodontal Health and Glycemic Control in Diabetic Patients: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 6 Oct 2026

Brief summary (registry, in English)

This randomized controlled clinical trial aims to evaluate the effectiveness of a para-probiotic-based oral care protocol in improving periodontal health and glycemic control in patients with type 2 diabetes mellitus (T2DM). A total of 40 adult patients (aged 18-70) with diagnosed periodontitis and T2DM will be enrolled and randomly assigned to two treatment groups. Both groups will receive standard non-surgical periodontal therapy. The test group will use para-probiotic toothpaste and mouthwash (Biorepair Plus Parodontogel and Biorepair Plus mouthwash) twice daily for 15 days after each recall visit, while the control group will use toothpaste and mouthwash containing 0.20% chlorhexidine on the same schedule. Clinical evaluations will be conducted at baseline (T0), 3 months (T1), and 6 months (T2), assessing key periodontal parameters including clinical attachment level (CAL), bleeding on probing (BoP), probing pocket depth (PPD), plaque index (PI), and glycemic control via hemoglobin A1c (HbA1c) levels. Patient satisfaction with treatment will be assessed using a questionnaire at T1 and T2. The primary objective is to evaluate the change in CAL from baseline to 6 months. Secondary objectives include the evaluation of changes in BoP, PPD, PI, HbA1c, and patient-reported satisfaction. This study seeks to determine whether para-probiotic oral care products can offer clinical benefits for periodontal disease management and systemic glycemic control in diabetic patients, potentially serving as a natural adjunct to conventional periodontal therapy.

Status (registry)
Completed
Study type
Interventional
Enrollment
40 (actual)
First submitted
5 Jul 2025
Start date
30 Jul 2025
Primary completion date
1 Jun 2026
Lead sponsor
University of Pavia
NCT number
NCT07069166

What you commit to

  • Study type: Interventional
  • Participants enrolled: 40
  • From 30 Jul 2025 to the primary completion date, 1 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Presence of cardiac pacemakers
  • History of neurological disorders
  • History of psychiatric disorders
  • Steroid-induced diabetes mellitus

Other

  • Current pregnancy or breastfeeding
  • Inability or unwillingness to attend follow-up visits or adhere to home oral care instructions

Who the study is looking for

  • Age between 18 and 70 years
  • Diagnosis of periodontitis (Stage II or III; Grade B or C)
  • Presence of at least one periodontal pocket per side of the mouth, with a maximum of 20 teeth presenting pathological probing depths
  • Presence of both single- and multi-rooted teeth
  • Type 2 diabetes mellitus diagnosed at least one year prior to enrollment
  • Good general health status and ability to comply with study protocol
  • Written informed consent provided

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Unit of Orthodontics and Pediatric Dentistry - Section of Dentistry - Department of Clinical, Surgical, Diagnostic and Pediatrics - University of Pavia
Coordinator of this site? Confirm its status
PaviaItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.