Antibacterial Photodynamic Therapy in the Management of Peri-implantitis

Recruiting now · Not applicable

Conditions studied: Peri-Implantitis, Plaque, Dental

In brief

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.

Key facts

Study ID

NCT06017817

Run by

Koite Health Oy

People needed

80

Starts

2024-05-13

Expected to finish

2026-12-31

Last updated by the study team

2026-08-07

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• Presence of any physical limitation or restriction that might restrict Lumoral use
• Unwilling to participate in the study
• Pregnancy or lactation
• Active smoking
• Medicated diabetes mellitus (DM)
• Any systemic disease (e.g., wound healing dysfunctions) that could alter the progression of peri-implantitis
• Use of antibiotics and doxycycline, chlorhexidine, and bisphosphonates, within 4 weeks week prior to study participation
• Peri-implant and periodontal treatment within 3 months prior to study participation
• Removable major prosthesis or major orthodontic appliance

Where it is running

• Södertandläkarna AB — Stockholm, Sweden (enrolling)

Full record on ClinicalTrials.gov

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