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Regular Home-use of Dual-light Photodynamic Therapy in the Management of Chronic Stage III-IV Periodontitis

Sponsored by Koite Health Oy

About this trial

Last updated 2 years ago

Study ID

LumoKaunas2023

Status

Recruiting

Type

Interventional

Phase

N/A

Placebo

No

Accepting

18-75 Years
18 to 85 Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Started 2 years ago

What is this trial about?

This study is designed to determine the efficacy of the Lumoral method in chronic periodontitis with a targeted group of stage III and IV periodontitis. Improved supragingival plaque control can help to also sustain the subgingival plaque management in the long term. In addition, the method might have a photobiomodulation effect on periodontal tissues.

What are the participation requirements?

Yes

Inclusion Criteria

- Periodontal disease stage III-IV, according to criteria the American Academy of Periodontology (AAP) with at least 3 mm interdental clinical attachment level (CAL) in the site of greatest loss.

- ≥ 18 years old

- Presence of ≥20 teeth, including implants

- 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

No

Exclusion Criteria

- Grade A or C periodontitis

- Presence of any physical limitation or restriction that might restrict Lumoral use

- Pregnancy or lactation

- Active smoking

- Medicated diabetes mellitus (DM)

- Any systemic disease (e.g., wound healing dysfunctions) that could alter the progression of periodontal disease

- Use of antibiotics within 4 weeks week prior study

- Periodontal treatment within 3 months prior study

- Removable major prosthesis or major orthodontic appliance

- A need for a hopeless teeth extraction, or open cavities in need for immediate endodontic treatment

Locations

Location

Status

Recruiting