Awardee OrganizationBOSTON UNIVERSITY MEDICAL CAMPUS
Description
Abstract Text
This is a multicenter, randomized, double-blind, placebo controlled, 24 month study with 6 and 12 month interim analyses to evaluate the efficacy, safety, and tolerability of weekly oral Alendronate 70 mg on alveolar crestal height and clinical attachment level in men and women with moderate to severe periodontal disease in the absence of scaling and root planning. Disease progression will be frequently monitored and mechanical therapy administered if clinically indicated. Eligible patients will be randomly allocated to 1 of 2 treatment groups.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
alendronateclinical researchclinical trialsdental disorder chemotherapydrug screening /evaluationgender differencehuman subjecthuman therapy evaluationlongitudinal human studymedical complicationoral administrationpathologic bone resorptionpathologic processperiodontium disorder
No Sub Projects information available for 5M01RR000533-32 0345
Publications
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Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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History
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Similar Projects
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