Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06486012

Regular Use of aPDT in the Management and Prevention of Periodontitis Symptoms in Diabetic Patients

Led by Wellbeing Services County of Pirkanmaa · Updated on 2025-08-06

150

Participants Needed

1

Research Sites

201 weeks

Total Duration

On this page

Sponsors

W

Wellbeing Services County of Pirkanmaa

Lead Sponsor

T

Tampere University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This is an investigator-initiated clinical study to establish easy referral and access for diabetic patients from primary health care to oral health care facilities for preventive oral care, periodontal assessment, and treatment, and to investigate the impact of regular home use of aPDT medical device on plaque control and gingival health, when used as an adjunct treatment to standard oral hygiene, and the effect on diabetes control in patients with the risk of periodontal disease, compared to a standard home care oral hygiene regimen.

CONDITIONS

Official Title

Regular Use of aPDT in the Management and Prevention of Periodontitis Symptoms in Diabetic Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diabetic patient treated at community health care
  • At least 18 years old
  • Presence of 620 teeth
  • Agreement to participate in the study and sign a written consent form
  • Ability to cooperate with the treatment protocol according to coordinator investigator's assessment
Not Eligible

You will not qualify if you...

  • Oral thrush
  • Known sensitivity to near-infrared or antibacterial blue light

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Wellbeing Services of County Pirkanmaa

Tampere, Pirkanmaa, Finland, 33520

Actively Recruiting

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Research Team

M

Miia Ehrnrooth

CONTACT

M

Mikko Kylmänen, Master of Health Care

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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