Prevention of Dental Implant Diseases

Sponsor
Hanna (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05871229
Collaborator
University of Helsinki (Other), Koite Health Oy (Industry), Hammasklinikka Kruunu (Other)
40
1
2
11.6
3.5

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Lumoral Treatment
  • Other: Standard treatment for peri-implantitis
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
RandomizedRandomized
Masking:
Double (Participant, Investigator)
Masking Description:
Participants will be randomized at the end of baseline visit
Primary Purpose:
Treatment
Official Title:
Prevention of Dental Implant Diseases: Early Diagnosis and Monitoring in Clinical Work and Enhanced Oral Health Maintenance at Home
Actual Study Start Date :
Jan 13, 2023
Anticipated Primary Completion Date :
Jun 30, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Study group

Lumoral and standard treatment

Device: Lumoral Treatment
Photodynamic antibacterial dual-light device with a marker substance

Other: Standard treatment for peri-implantitis
Standard treatment for peri-implantitis as per international, national and clinic guidelines

Other: Control group

Standard treatment only

Other: Standard treatment for peri-implantitis
Standard treatment for peri-implantitis as per international, national and clinic guidelines

Outcome Measures

Primary Outcome Measures

  1. Active matrix metalloproteinase 8 (aMMP-8) [30 days]

    Change in periodontal inflammation marker aMMP-8

Secondary Outcome Measures

  1. Bleeding on probing (BOP) [30 days]

    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

  2. Visible plaque index (VPI) [30 days]

    Change in visible plaque index

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hammasklinikka Kruunu Oy Tampere Pirkanmaa Finland 33200

Sponsors and Collaborators

  • Hanna
  • University of Helsinki
  • Koite Health Oy
  • Hammasklinikka Kruunu

Investigators

  • Principal Investigator: Hanna Lähteenmäki, Doctor, Hammasklinikka Kruunu

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Hanna, PhD, Dental Hygienist, Koite Health Oy
ClinicalTrials.gov Identifier:
NCT05871229
Other Study ID Numbers:
  • IS-TRE
First Posted:
May 23, 2023
Last Update Posted:
May 23, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hanna, PhD, Dental Hygienist, Koite Health Oy
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 23, 2023