Periodontitis Clinical Trial
Official title:
A Multicenter, Randomized, Examiner Blinded Study of Photoactivated Disinfection 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 planning (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 | Completed |
Enrollment | 40 |
Est. completion date | January 2007 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. The subject is capable of giving informed consent 2. The subject is willing to sign a consent form 3. The subject is an adult male or female > 18 4. The subject is diagnosed with chronic periodontitis 5. The subject has >18 fully erupted teeth 6. The subject has at least 4 measurement sites with pocket depth of 6-9 mm in at least two quadrants of the mouth. 7. Subject is willing and able to return for treatment and evaluation procedures scheduled throughout the course of this clinical study Exclusion Criteria: 1. The subject is pregnant or nursing or who plans to become pregnant in the next 4 months 2. The subject has significant liver disease by subject report 3. The subject has an active malignancy of any type by subject report 4. The subject has chronic disease or diminished mental capacity that would mitigate the ability to comply with the protocol 5. The subject has any significant disease (either acute or chronic) or who is taking a medication with concomitant oral manifestations that in the opinion of the investigator would interfere with evaluation of safety or efficacy of PERIOWAVE® 6. The subject has an active periapical abscess or periodontal abscess or a history of acute necrotizing ulcerative gingivitis 7. The subject has been treated 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. The subject has a known allergy to Methylene Blue 9. Has glucose-6-phosphate dehydrogenase (G6PD) deficiency by subject report 10. The subject currently uses anti-coagulant therapy at therapeutic doses 11. The subject is currently using any photosensitizing medications 12. The subject has participated in investigational treatment in the last 30 days or has the expectation for using a separate investigational treatment during the time of the study 13. The subject has smoked tobacco products in the last year |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Canada | Office of Dr. Sonia Leziy | North Vancouver | British Columbia |
Canada | University of British Columbia School of Dentistry | Vancouver | British Columbia |
Lead Sponsor | Collaborator |
---|---|
Ondine Research Laboratories |
Canada,
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* Note: There are 43 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 | Reduction in Periodontal Pocket Depth | 6, 12 weeks | ||
Secondary | Reduction in Bleeding on Probing | 6, 12 weeks |
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