Biomarkers of Periodontal Disease Progression
This trial is active, not recruiting.
|Sponsor||The Forsyth Institute|
|Collaborator||National Institute of Dental and Craniofacial Research (NIDCR)|
|Start date||January 2012|
|End date||June 2016|
|Trial size||500 participants|
|Trial identifier||NCT01489839, 10-174-E, 5U01DE021127-02|
The primary purpose of the study will be to look for biological biomarkers to determine which people with gum disease will have a worsening of the disease. A second objective of this study will be to look at the effects of periodontal treatment on the levels of the biomarkers that are identified.
|United States||No locations recruiting|
|Other countries||No locations recruiting|
|Edwardsville, IL||Southern Illinois University||no longer recruiting|
|Cambridge, MA||The Forsyth Institute||no longer recruiting|
|Ann Arbor, MI||University of Michigan School of Dentistry||no longer recruiting|
|Buffalo, NY||State University of New York at Buffalo||no longer recruiting|
|New York, NY||NYU College of Dentistry||no longer recruiting|
Change in Clinical Attachment Level (CAL)
time frame: After the baseline visit, subjects will return to the clinic every 2 months (± 7 days relative to baseline) for 12 months.
Biomarker Levels compared between progressing and non-progressing sites as determined by CAL changes
time frame: Levels measured every 2 months for 12 months
Male or female participants at least 25 years old.
Inclusion Criteria: General Inclusion Criteria To be eligible to participate in this study, a subject must meet all of the following criteria: 1. Ability to understand, and willingness and ability to read and sign, the informed consent form. 2. Age of at least 25 years. 3. Ability to understand and follow directions for study procedures. 4. Minimum of 20 natural teeth, excluding third molar teeth; at least 12 of these teeth must be pre-molars, first molars, or second molars. 5. Willingness not to have professional dental prophylaxis or scaling for the duration of the disease progression and monitoring phase (12 months). 6. Willingness to comply with all study procedures and be available for the duration of the study. 7. For women with reproductive potential, willingness to use highly effective contraception (e.g., licensed hormonal contraception, intrauterine device, abstinence, or vasectomy in partner). Specific inclusion criteria: Healthy periodontal subjects must have: 1. Any tooth with 3 mm or less PD, irrespective of the attachment level, will be acceptable 2. No teeth with PD of 4 mm or more and concomitant attachment loss, with the exception of the distal of the second molars where a PD of 4 mm and concomitant CAL of up to 2 mm will be acceptable. 3. No radiographic evidence of alveolar bone loss (defined as a distance of greater than 2.0 mm measured radiographically from the CEJ to the crest of the alveolar bone); with the exception of the mandibular incisors where up to 3.0 mm of alveolar bone loss measured radiographically from the CEJ to the crest of the alveolar bone will be accepted. Mild periodontal disease subject: periodontal loss must meet the following criteria and must not meet the minimum criteria for severe periodontal loss: 1. At least 4 teeth with at least 1 site of PD of 5 mm or more and concomitant CAL greater than or equal to 2 mm, and radiographic evidence of mesial or distal alveolar bone loss around at least 2 of the affected teeth. Alveolar bone loss is defined as a distance of > 2.0 mm measured radiographically from the CEJ to the crest of the alveolar bone. Subjects with severe periodontal loss must meet all of the following criteria: 1. At least 8 separate teeth with at least 1 site of PD of 5 mm or more and concomitant CAL greater than or equal to 3 mm, and radiographic evidence of mesial or distal alveolar bone loss around at least 2 of the affected teeth. Alveolar bone loss is defined as a distance of > 2.0 mm measured radiographically from the CEJ to the crest of the alveolar bone. Exclusion Criteria: 1. Presence of orthodontic appliances. 2. The following conditions noted on oral examination: - Oral lichen planus - Candidiasis - Clinical leukoplakia - Clinical erythroplakia - Pemphigus - Pemphigoid - Other recurrent intraoral or perioral vesiculobullous diseases - Aphthous ulcerations (major or minor). Subjects presenting with aphthous ulcers should be rescreened after 2 weeks. They will be eligible if the ulcers have healed and the subject does not have a history of frequent recurrences. - Herpetic lesions. Subjects presenting with herpes labialis or intraoral herpes should be rescreened after 2 weeks. They will be eligible if the lesions have healed and the subject does not have a history of frequent recurrences. j. Traumatic ulcers. If a subject presents with a traumatic ulcer, he/she can be rescreened in 2-3 weeks. The subject will be eligible if the ulcers have healed. 3. Acute necrotizing ulcerative gingivitis or gross tooth decay, as determined by the investigator. 4. Root fragments, pericoronitis, endo-perio lesions, or other dental abscesses. Subjects may be rescreened after resolution of these dental conditions. 5. Pregnancy or lactation. 6. Requirement for prophylactic antibiotics for dental procedures (e.g., for certain heart and orthopaedic conditions*). 7. Periodontal or systemic antibiotic therapy in the previous 6 months. Routine dental prophylaxis will be allowed. 8. Use of cigarettes or other tobacco products within 1 year before the screening visit. 9. Any medical condition that might influence the course of periodontal disease or treatment (e.g., diabetes [irrespective of level of control], human immunodeficiency virus infection or acquired immunodeficiency syndrome, use of medications associated with gingival hyperplasia). 10. Chronic use of nonsteroidal anti-inflammatory drugs (e.g., for arthritis), defined as the need, or anticipated need, for over 3 weeks of continuous use at the time of enrollment or during the course of the study. The use of low-dose aspirin (81 mg/day) for prophylaxis will be allowed. 11. Current or anticipated use of chronic systemic corticosteroids, cyclosporine, or other systemic immunosuppressive agent. The use of inhaled corticosteroids will be allowed. 12. Hypersensitivity to tetracyclines (e.g., tetracycline, doxycycline, minocycline). 13. Participation in a clinical study testing a drug, biologic, device, or other intervention within the last 30 days. 14. Any condition or circumstance that, in the opinion of the investigator, would place the subject at increased risk or preclude his/her full compliance with or completion of the study.
|Official title||Biomarkers of Periodontal Disease Progression|
|Principal investigator||Ricardo P Teles, DDS, DMSc|
|Description||This multicenter clinical study will investigate biomarkers of periodontal disease progression. The study will enroll 375 subjects with periodontal disease and 125 periodontally healthy subjects. All subjects will be monitored clinically and have samples taken every 2 months for 12 months for analysis of inflammatory and immunological biomarkers and microbial species. Subjects displaying periodontal disease progression greater than an established threshold will receive periodontal rescue therapy at progressing periodontal sites and continue with monitoring. Periodontally healthy subjects and non-progressing sites in subjects with periodontal disease will serve as controls. After 12 months, subjects with periodontal disease will receive periodontal therapy consisting of 4 quadrants of scaling and root planing. Periodontally healthy subjects will receive prophylaxis and scaling and exit the study. Following periodontal therapy, subjects with periodontal disease will be followed for a maintenance period of 6 months for clinical and biological monitoring. Statistical analyses will compare biomarkers and microbial species between periodontally healthy subjects and subjects with periodontal disease, between progressing and non-progressing periodontally diseased sites, and between periodontally diseased sites before and after periodontal therapy.|
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