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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05698823
Other study ID # LumoKaunas2023
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 6, 2023
Est. completion date December 31, 2027

Study information

Verified date April 2024
Source Koite Health Oy
Contact Mikko Kylmänen, Bachelor
Phone +358407245934
Email mikko.kylmanen@koitehealth.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

The Lumoral Treatment is a CE-marked medical device developed to provide a potent, targeted antibacterial action on dental plaque in a home environment. The device mechanism of action is antibacterial photodynamic therapy (aPDT). The device is used by swishing a specially designed mouth rinse that strongly adheres to dental plaque. The plaque-adhered photoactive mouth rinse can be activated by a simple-to-use light applicator. Preliminary results have shown promising anti-inflammatory responses in addition to plaque reduction.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 31, 2027
Est. primary completion date May 31, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility 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 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

Study Design


Related Conditions & MeSH terms

  • Periodontitis
  • Periodontitis Chronic Generalized Moderate
  • Periodontitis Chronic Generalized Severe

Intervention

Device:
Lumoral Treatment
The Lumoral treatment -device is a CE-marked antibacterial home-use device for the treatment and prevention of oral diseases caused by bacteria. It is used in combination with a CE-marked mouth rinse called Lumorinse.

Locations

Country Name City State
Lithuania Hospital of Lithuanian University of Health Sciences Kaunas Clinics, Department of Dental and Oral Pathology Kaunas

Sponsors (3)

Lead Sponsor Collaborator
Koite Health Oy Lithuanian University of Health Sciences, University of Helsinki

Country where clinical trial is conducted

Lithuania, 

References & Publications (5)

Kassebaum NJ, Bernabe E, Dahiya M, Bhandari B, Murray CJ, Marcenes W. Global burden of severe periodontitis in 1990-2010: a systematic review and meta-regression. J Dent Res. 2014 Nov;93(11):1045-53. doi: 10.1177/0022034514552491. Epub 2014 Sep 26. — View Citation

Kassebaum NJ, Smith AGC, Bernabe E, Fleming TD, Reynolds AE, Vos T, Murray CJL, Marcenes W; GBD 2015 Oral Health Collaborators. Global, Regional, and National Prevalence, Incidence, and Disability-Adjusted Life Years for Oral Conditions for 195 Countries, 1990-2015: A Systematic Analysis for the Global Burden of Diseases, Injuries, and Risk Factors. J Dent Res. 2017 Apr;96(4):380-387. doi: 10.1177/0022034517693566. — View Citation

Lang NP, Suvan JE, Tonetti MS. Risk factor assessment tools for the prevention of periodontitis progression a systematic review. J Clin Periodontol. 2015 Apr;42 Suppl 16:S59-70. doi: 10.1111/jcpe.12350. — View Citation

Nikinmaa S, Moilanen N, Sorsa T, Rantala J, Alapulli H, Kotiranta A, Auvinen P, Kankuri E, Meurman JH, Patila T. Indocyanine Green-Assisted and LED-Light-Activated Antibacterial Photodynamic Therapy Reduces Dental Plaque. Dent J (Basel). 2021 May 3;9(5):52. doi: 10.3390/dj9050052. — View Citation

Slade GD. Derivation and validation of a short-form oral health impact profile. Community Dent Oral Epidemiol. 1997 Aug;25(4):284-90. doi: 10.1111/j.1600-0528.1997.tb00941.x. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Device-related adverse event Absence of device-related serious adverse events or any patterns of device-related adverse events graded as moderate 6 months
Primary Bleeding on probing (BOP) Improvement in bleeding on probing (BOP)
A full-mouth assessment at six sites per tooth (mesiobuccal, buccal, distobuccal, mesiolingual, lingual, distolingual)
Gingival bleeding is considered as positive if bleeding occurs within 15 seconds after gentle probing with a probe at the sulcus
Dichotomous scoring to each site of the tooth as bleeding "1 present" and "0 absent"
BOP is reported as the percentage (%) of sites with positive findings
Calculation formula: number of bleeding sites/ 6 times number of teeth
6 months
Secondary Active matrix metalloproteinase 8 (aMMP-8) Change in periodontal inflammation marker aMMP-8 6 months
Secondary Visible plaque index (VPI) Change in visible plaque index (VPI) 6 months
Secondary Probing pocket depth (PPD) Change in probing pocket depth (PPD) 6 months
Secondary Clinical attachment level (CAL) Change in clinical attachment level (CAL) 6 months
Secondary Deep periodontal pockets (over 4 mm) Change in the number of deep periodontal periodontal pockets (over 4 mm) 6 months
Secondary Periodontal microbiological flora Change in periodontal microbiological flora during the study period 6 months
Secondary Additional visits Number of additional visits due to periodontitis status between 2nd and 3rd follow-up visits 6 months
Secondary OHIP-14 Patient related objectives: Oral-related quality of life measurement (OHIP-14) questionnaire 6 months
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