Chronic Periodontitis Clinical Trial
Official title:
1.2% Rosuvastatin Gel As A Local Drug Delivery Agent In Smokers With Chronic Periodontitis- A Randomized Controlled Clinical Trial.
Verified date | February 2017 |
Source | Government Dental College and Research Institute, Bangalore |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the present study was to evaluate the effects of subgingival delivery of Rosuvastatin gel as an adjunct to scaling and root planing in Smokers With Chronic Periodontitis (CP) patients.
Status | Completed |
Enrollment | 60 |
Est. completion date | April 2016 |
Est. primary completion date | April 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 30 Years to 50 Years |
Eligibility |
Inclusion Criteria: - Systemically healthy CP subjects aged between 30-50 years who are current smokers with no history of periodontal therapy or use of antibiotics in past 6 months, having sites with intrabony defect depth (IBD) = 3mm (distance between alveolar crest and base of the defect on intraoral periapical radiograph) along with PPD =5 mm or CAL =3 mm in an asymptomatic tooth were included in the study. A subject was considered as a current smoker if he regularly smoked more than 10 cigarettes/day for a minimum of 5 years Exclusion Criteria: - Former smokers, i.e. subjects who had previously been smokers but stopped their habit, and non-smokers were excluded. Subjects allergic to statins, on systemic statin therapy, with any known systemic disease or any other systemic inflammation/ infection which could alter the course of periodontal disease and users of tobacco in any other form than cigarettes were excluded from the study |
Country | Name | City | State |
---|---|---|---|
India | Government Dental College and Research Institute | Bangalore | Karnataka |
Lead Sponsor | Collaborator |
---|---|
Government Dental College and Research Institute, Bangalore |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Defect depth reduction (%) | assessed in percentage | Change from baseline to 9 months | |
Secondary | probing depth (mm) | measured in mm | Change from baseline to 9 months | |
Secondary | clinical attachment level (mm) | measured in mm | Change from baseline to 9 months | |
Secondary | modified sulcus bleeding index | scale from 0-3 | Change from baseline to 9 months | |
Secondary | Plaque Index | scale from 0-3 | Change from baseline to 9 months |
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