Prevention of Dental Implant Diseases

Hanna Lähteenmäki

Status: Completed

Conditions: Peri-Implantitis

Treatments: Other: Standard treatment for peri-implantitis; Device: Lumoral Treatment

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05871229

IS-TRE

Details and patient eligibility

About

The aim of this study is to determine the effect of regular antibacterial photodynamic Lumoral® treatment on gingival health and plaque volume, and anti-inflammatory effect of daily double light therapy on implant teeth. The study will use a medical device containing a light-activated Lumorinse® mouthwash and a Lumoral® light activator.

Full description

The hypothesis is that antibacterial photodynamic therapy improves tissue health by reducing inflammation without any side effect.

Study participants will be invited from a dental clinic in Tampere, Finland, from the patients of an oral hygienist's office. Participants will be randomized to the treatment and control groups using the closed envelope method. Participants in the treatment group will receive Lumoral® treatment according to the manufacturer's protocol, once daily for 10 min for 15 days and then twice daily for 15 days.

Enrollment: 40 patients

Sex: All

Ages: 25+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• One or more dental implants
• Diagnosis of peri-implantitis
• Challenges in keeping high self-care oral care standards
• Over 25 years of age

Exclusion criteria

• Any antibiotic medication within 6 months prior to study participation

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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40 participants in 2 patient groups

Study group

Experimental group

Description:

Lumoral and standard treatment

Treatment:

Device: Lumoral Treatment

Other: Standard treatment for peri-implantitis

Control group

Other group

Description:

Standard treatment only

Treatment:

Other: Standard treatment for peri-implantitis