Periodontitis Clinical Trial
Official title:
Photodynamic Disinfection in Combination With Scaling and Root Planing in the Treatment of Chronic Periodontitis
Verified date | May 2007 |
Source | Ondine Research Laboratories |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Ethics Review Committee |
Study type | Interventional |
This study is to determine whether scaling and root planing (SRP) followed by photodynamic disinfection results in improved outcomes that persist over time in adults with chronic periodontitis when compared with subjects with SRP alone.
Status | Active, not recruiting |
Enrollment | 120 |
Est. completion date | October 2007 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Adult male or female over the age of 18 2. Having been diagnosed with chronic periodontitis 3. >18 fully erupted teeth 4. Has had no periodontal instrumentation in the four months prior to initiation of study treatment 5. Subject has at least 4 sites with pocket depth of 6-9 mm in at least two quadrants of the mouth. 6. Subject is willing and able to return for treatment and evaluation procedures scheduled throughout the course of this clinical study 7. The subject is capable of giving informed consent 8. Subject is willing to sign a consent form Exclusion Criteria: 1. Is pregnant or nursing or who plans to become pregnant in the next 4 months 2. Having significant liver disease by subject report 3. Having an active malignancy of any type by subject report 4. Having chronic disease or diminished mental capacity that would mitigate the ability to comply with the protocol 5. Having any significant disease (either acute or chronic) or who is taking medication with concomitant oral manifestations that in the opinion of the investigator would interfere with evaluation of safety or efficacy of PerioWave® 6. Having an active periapical abscess or periodontal abscess or a history of acute necrotizing ulcerative gingivitis 7. Treatment with antibiotics within the 1-month period prior to beginning the study or any systemic condition which requires antibiotic coverage for routine periodontal procedures (e.g. heart conditions, joint replacements, etc) by report of the subject 8. Known allergy to methylene blue 9. Has glucose-6-phosphate dehydrogenase (G6PD) deficiency by subject report 10. Currently uses anti-coagulant therapy at therapeutic doses 11. Currently uses photosensitizing medications 12. Participated in investigational treatment in the last 30 days or expectation for using a separate investigational treatment during the time of the study |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Canada | University of Alberta | Edmonton | Alberta |
Canada | University of Western Ontario | London | Ontario |
Canada | University of Saskatchewan | Saskatoon | Saskatchewan |
Canada | North York Dental Center | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
Ondine Research Laboratories |
Canada,
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* Note: There are 45 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Increase in clinical attachment level | 6, 12 weeks | ||
Secondary | Decrease in periodontal pocket depth | 6, 12 weeks | ||
Secondary | Reduction in bleeding on probing | 6, 12 weeks |
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