Plaque Clinical Trial
Official title:
Effect of Regular Antibacterial Photodynamic Therapy on Oral Hygiene in the Elderly 24-hour Care Residents
Verified date | February 2024 |
Source | Koite Health Oy |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aims to determine the effectiveness of the Lumoral device on oral hygiene, inflammatory load, and dryness of mouth in elderly 24-hour care residents. The second aim is to investigate the usefulness and benefits of the aMMP-8 chair-side test and the Lumoral device in improving the oral hygiene of elderly people. In addition, the study will investigate the usability of Lumoral assessed by different care professionals to evaluate the need for oral care and plaque control procedures in elderly residents.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 31, 2026 |
Est. primary completion date | October 31, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - A 24-hour care resident; - Understand and able to give consent to the study; - At least 10 functional teeth in the mouth (including implants); - Able to brush teeth and follow the instruction for use Lumoral treatment, based on the assessment by the nursing staff. Exclusion Criteria: - Incapable of participating in the study based on the assessment of the nursing staff - Toothless or less than 10 functional teeth in the mouth (including implants) - Unwilling or unable to give consent |
Country | Name | City | State |
---|---|---|---|
Sweden | Pilträdets servicehus | Stockholm |
Lead Sponsor | Collaborator |
---|---|
Koite Health Oy | Karolinska Institutet, University of Helsinki |
Sweden,
De Visschere L, de Baat C, De Meyer L, van der Putten GJ, Peeters B, Soderfelt B, Vanobbergen J. The integration of oral health care into day-to-day care in nursing homes: a qualitative study. Gerodontology. 2015 Jun;32(2):115-22. doi: 10.1111/ger.12062. Epub 2013 Jun 20. — View Citation
Holmen A, Stromberg E, Hagman-Gustafsson ML, Wardh I, Gabre P. Oral status in home-dwelling elderly dependent on moderate or substantial supportive care for daily living: prevalence of edentulous subjects, caries and periodontal disease. Gerodontology. 2012 Jun;29(2):e503-11. doi: 10.1111/j.1741-2358.2011.00507.x. Epub 2011 Sep 19. — View Citation
Hugoson A, Koch G, Gothberg C, Helkimo AN, Lundin SA, Norderyd O, Sjodin B, Sondell K. Oral health of individuals aged 3-80 years in Jonkoping, Sweden during 30 years (1973-2003). II. Review of clinical and radiographic findings. Swed Dent J. 2005;29(4):139-55. — View Citation
Lahteenmaki H, Patila T, Raisanen IT, Kankuri E, Tervahartiala T, Sorsa T. Repeated Home-Applied Dual-Light Antibacterial Photodynamic Therapy Can Reduce Plaque Burden, Inflammation, and aMMP-8 in Peri-Implant Disease-A Pilot Study. Curr Issues Mol Biol. 2022 Mar 8;44(3):1273-1283. doi: 10.3390/cimb44030085. — View Citation
Nikinmaa S, Alapulli H, Auvinen P, Vaara M, Rantala J, Kankuri E, Sorsa T, Meurman J, Patila T. Dual-light photodynamic therapy administered daily provides a sustained antibacterial effect on biofilm and prevents Streptococcus mutans adaptation. PLoS One. 2020 May 6;15(5):e0232775. doi: 10.1371/journal.pone.0232775. eCollection 2020. — 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
Nikinmaa S, Podonyi A, Raivio P, Meurman J, Sorsa T, Rantala J, Kankuri E, Tauriainen T, Patila T. Daily Administered Dual-Light Photodynamic Therapy Provides a Sustained Antibacterial Effect on Staphylococcus aureus. Antibiotics (Basel). 2021 Oct 13;10(10):1240. doi: 10.3390/antibiotics10101240. — View Citation
Nishizawa T, Niikura Y, Akasaka K, Watanabe M, Kurai D, Amano M, Ishii H, Matsushima H, Yamashita N, Takizawa H. Pilot study for risk assessment of aspiration pneumonia based on oral bacteria levels and serum biomarkers. BMC Infect Dis. 2019 Sep 2;19(1):761. doi: 10.1186/s12879-019-4327-2. — View Citation
Saarela RKT, Hiltunen K, Kautiainen H, Roitto HM, Mantyla P, Pitkala KH. Oral hygiene and health-related quality of life in institutionalized older people. Eur Geriatr Med. 2022 Feb;13(1):213-220. doi: 10.1007/s41999-021-00547-8. Epub 2021 Jul 27. — View Citation
Saarela RKT, Hiltunen K, Mantyla P, Pitkala KH. Changes in Institutionalized Older People's Dentition Status in Helsinki, 2003-2017. J Am Geriatr Soc. 2020 Jan;68(1):221-223. doi: 10.1111/jgs.16230. Epub 2019 Oct 26. No abstract available. — View Citation
Suominen AL, Varsio S, Helminen S, Nordblad A, Lahti S, Knuuttila M. Dental and periodontal health in Finnish adults in 2000 and 2011. Acta Odontol Scand. 2018 Jul;76(5):305-313. doi: 10.1080/00016357.2018.1451653. Epub 2018 Mar 16. — View Citation
Willumsen T, Karlsen L, Naess R, Bjorntvedt S. Are the barriers to good oral hygiene in nursing homes within the nurses or the patients? Gerodontology. 2012 Jun;29(2):e748-55. doi: 10.1111/j.1741-2358.2011.00554.x. Epub 2011 Oct 24. — View Citation
* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Oral hygiene | Improvement in oral hygiene / resident experience. The study subject will fill in a questionnaire related to oral hygiene and mouth dryness at baseline and at 2 months. | 2 months | |
Primary | Visual Plaque Index (VPI) | Change in the Visible plaque index (VPI) is greater in the Study group compared to the Control group.
VPI: A full-mouth assessment at 4 sites per tooth will be made at baseline and at the 2 month follow-up visit VPI is reported as the percentage (%) of sites with positive findings Dichotomous scoring to each site of the tooth as plaque" 1 present" and" 0 absent" Calculation formula: number of plaque sites/ 4 times number of teeth |
2 months | |
Primary | Bleeding on Probing (BOP) | Change in the Bleeding on Probing (BOP) is greater in the Study group compared to the Control group.
BOP: A full-mouth assessment at 4 sites per tooth Gingival bleeding is considered as positive if bleeding occurs within 15 seconds after gentle probing with a probe at the sulcus BOP reported as the percentage (%) of sites with positive findings Dichotomous scoring to each site of the tooth as bleeding" 1 present" and" 0 absent" Calculation formula: number of bleeding sites/ 4 times number of teeth |
2 months | |
Primary | Probing Pocket Depth (PPD) | Change in the Probing Pocket Depth (PPD) values is greater in the Study group compared to the Control group.
PPD: A full-mouth assessment, measured at 4 sites per tooth Assessed from the base of the pocket to the gingival margin (mm) |
2 months | |
Primary | aMMP-8 | Change in the active matrix metalloproteinase 8 values is greater in the Study group compared to the Control group.
The aMMP-8 marker analysis will be performed using the Periosafe chair-side test (Dentognostics GmbH) according to the manufacturer's instructions. Oral rinse samples will be stored for further analysis according to the Swedish Biobanks in Medical Care Act (SFS 2002:297). Further analysis includes aMMP-8 and its regulators by biochemical enzyme/molecule assays, immunoassays, and proteomics analysis. |
2 months | |
Primary | Dry mouth | Use of the Lumoral Treatment relieves the symptoms of dry mouth, compared to the Control group.
Clinical assessment of moisture/dryness of oral mucosa (score 0-2) 0 = Saliva secretion looks normal (saliva serous and running) = Mucous membrane of the mouth shiny and tightening/ saliva foamy or mucous/ little clear saliva at the base of the mouth = Mouth completely dry, mirror sticking to cheek or tongue, mucous membranes often reddened/ bumps on tongue surface disappeared/ scab on melting |
2 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02377310 -
Pd/Pa vs iFRâ„¢ in an Unselected Population Referred for Invasive Angiography
|
N/A | |
Completed |
NCT02980497 -
Antiplaque/Antigingivitis Efficacy of Essential Oil Mouthrinses in Six-Month Study
|
N/A | |
Not yet recruiting |
NCT03877705 -
Xylitol Chewable Tablets Versus Xylitol Chewing Gum in Geriatric Bedridden Patients
|
Early Phase 1 | |
Completed |
NCT02666508 -
Trial of Toothpaste to Reduce Plaque and Inflammation
|
N/A | |
Completed |
NCT04921371 -
Six Week Study of Experimental Mouth Rinses: Effect on Gingivitis and Plaque
|
Phase 1 | |
Completed |
NCT05138978 -
Metagenomic and Metatranscriptomic Analysis of Clinical Plaque Samples
|
Phase 2 | |
Completed |
NCT05428189 -
Efficacy of the Disclosing Plaque Agent as a Guide to Remove the Oral Biofilm in Orthodontic Patients.
|
N/A | |
Not yet recruiting |
NCT05031260 -
COMORAL® the Oral Irrigation Unit Clinical Trial
|
N/A | |
Completed |
NCT05091216 -
The Effects of Traditional Chinese Medicine Mouthwash Solutions on the Oral Health of Leprosy Patients
|
N/A | |
Active, not recruiting |
NCT03022344 -
DD2-Coronary Plaque Morphology and Plaque Progression
|
N/A | |
Completed |
NCT05121909 -
A Study of Experimental Mouthwashes
|
Phase 4 | |
Completed |
NCT06318819 -
Plaque Removal Effectiveness of a Flossing Device Compared to the Conventional Flossing in Adults
|
N/A | |
Completed |
NCT03989427 -
The Effectiveness of Brushing and Flossing Sequence on Control of Plaque and Gingival Inflammation
|
N/A | |
Completed |
NCT04407208 -
Convalescent Plasma Therapy in Patients With COVID-19
|
Phase 1 | |
Completed |
NCT05821712 -
A New Mouthwash on Reducing Dental Plaque and Helping Prevent Gum Problems
|
Phase 3 | |
Completed |
NCT05239351 -
Evaluating Performance and Safety of the Medical Device Jalucomplex in the Treatment of Facial and Neck Tissue Defects
|
N/A | |
Active, not recruiting |
NCT05239117 -
Evaluating the Performance and Safety of the Medical Device Plenhyage® in the Treatment of Dermal Tissue Defects
|
N/A | |
Completed |
NCT05120141 -
A Twelve Week Study of Experimental Mouth Rinses
|
Phase 4 | |
Active, not recruiting |
NCT05239130 -
Evaluating the Performance and Safety of the Medical Device Auralya® in the Treatment of Facial Dermal Tissue Defects
|
N/A | |
Completed |
NCT05239156 -
Evaluating the Performance and Safety of the Medical Device Janesse in the Treatment of Facial Dermal Tissue Defects
|
N/A |