Antibacterial Photodynamic Therapy in the Management of Peri-implantitis
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-85
SponsorNilminie Rathnayake
About this trial
This early-stage study is designed to determine the efficacy of the Lumoral method in periimplantitis. Improved supragingival plaque control can help to also sustain subgingival plaque management in the long term. In addition, the device might have a photobiomodulation effect on periodontal tissues, thus impacting osseointegration.
Eligibility criteria
Qualifiers
PPD ≥6 mm and marginal bone loss >3 mm
Dental implants collected and clinically characterized according to Lähteenmäki et al. CEDR-22
Agreement to participate in the study and to sign a written consent form
Able to co-operate with the treatment protocol and avoid any other oral hygiene measures outside of the study protocol
Disqualifiers
Presence of any physical limitation or restriction that might restrict Lumoral use
Unwilling to participate in the study
Pregnancy or lactation
Active smoking
Trial design
Treatments tested in this trial
- Lumoral Treatment
- Standard oral hygiene instructions
- Scaling and root planing (SRP
- surgical anti-infective peri-implantitis treatment
Treatment groups
80 Participants
are divided into 4 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov