Effect of Three Periodontal Therapies in Current Smokers and Non-Smokers
Information source: National Institute of Dental and Craniofacial Research (NIDCR)
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Periodontitis; Periodontal Diseases
Intervention: Group 1: metronidazole (Drug); Group 2: metronidazole + amoxicillin + locally delivered (Drug); Tetracycline (Drug); Metronidazole (Drug)
Phase: Phase 2
Status: Recruiting
Sponsored by: National Institute of Dental and Craniofacial Research (NIDCR) Official(s) and/or principal investigator(s): Anne Haffajee, DDS, Principal Investigator, Affiliation: Boston, MA
Summary
The purpose of this study is to determine in current and non-smokers the clinical and
microbiological effects of 3 therapies: scaling and root planing (SRP) alone; SRP in
combination with the orally administered antibiotic metronidazole; and SRP with the orally
administered antibiotics metronidazole and amoxicillin along with the locally delivered
antibiotic doxycycline at periodontal pockets >= 4 mm.
Clinical Details
Official title: Effect of Three Periodontal Therapies in Current Smokers and Non-Smokers
Study design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study
Primary outcome: Change in mean attachment level
Detailed description:
Cigarette smokers have more severe periodontal disease and more widespread colonization by
periodontal pathogens than non smokers. In addition, smokers respond less well to
periodontal therapies, particularly mechanical therapies such as scaling and root planing
(SRP) and surgery. Recent data from our laboratory have indicated that treatment that
included antibiotics produced a better clinical effect in smokers than mechanical therapy
alone. Thus, the purpose of the present investigation is to compare the immediate and
long-term effects of 3 periodontal therapies on clinical, microbiological and host parameters
in current and non smokers. In this double blind, placebo-controlled, randomized study, 108
current smokers and 108 non smokers will be randomly assigned to 1 of 3 treatment groups: SRP
alone; SRP + systemically administered metronidazole; SRP + systemically administered
amoxicillin and metronidazole and local delivery of doxycycline at pockets > 4 mm. Plaque
Index, Gingival Index, % of sites with bleeding on probing, suppuration, pocket depth and
attachment level will be measured at 6 sites per tooth at all teeth excluding 3rd molars at
baseline, 3, 6, 12, 18 and 24 months. Subgingival plaque samples taken from the mesial
aspect of each tooth at the same time points will be analyzed individually for their content
of 40 subgingival species using checkerboard DNA-DNA hybridization. Antibody levels to 20
subgingival species will be measured in serum samples taken at baseline, 6 and 24 months.
Levels of IL-1b, IL-10 and IFNg will be measured in GCF samples taken from the 4 deepest
pockets at baseline, 3, 6 and 24 months. The major hypothesis to be tested is whether
smokers respond better to periodontal therapies that include 1 or more antibiotics. Other
hypotheses will test whether host and microbiological parameters differ between smokers and
non smokers and if such parameters are comparably altered after therapy in both groups. The
results will be of immediate clinical benefit to the large segment of periodontal patients
who smoke cigarettes. Smokers make up 26 - 30% of the adult population and form a
disproportionately high segment of the population requiring periodontal treatment. They may
have special needs in terms of periodontal therapy which should be clarified by the proposed
investigation. In addition, the cigarette smoker is an example of a periodontal patient who
is "compromised" in terms of his/her ability to cope with infectious diseases. The proposed
investigation should provide a model to examine methods that could be useful in treating
compromised patients whether compromised by harmful habits such as smoking, systemic disease
or genetic background.
Eligibility
Minimum age: 20 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- > 20 teeth
- > 5% sites (approx. 8 sites) with pocket depth > 4 mm and / or 5% sites with
attachment level > 4 mm and mean AL < 4. 5 mm and mean PD < 3. 9 mm (not including tooth
brush abrasions).
Exclusion Criteria:
- > 50% of sites with pocket depth or attachment level > 4 mm
- Pregnancy or nursing
- Periodontal or antibiotic therapy in the previous 6 months
- Any systemic condition which might influence the course of periodontal disease or
treatment (e. g. diabetes, AIDS)
- Any systemic condition which requires antibiotic coverage for routine periodontal
procedures (e. g. heart conditions, joint replacements etc.)
- Liver disease
- Any known allergy to amoxicillin, metronidazole or doxycycline
- Lactose intolerance
Locations and Contacts
Department of Periodontology, Boston, Massachusetts 02115, United States; Recruiting Anne Haffajee, DDS, Phone: 617-262-5200, Ext: 243, Email: ahaffajee@forsyth.org Anne Haffajee, Principal Investigator
Additional Information
Starting date: July 2003
Ending date: April 2009
Last updated: July 15, 2008
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