Study of effect of dental gel in improving gum condition.
- Conditions
- Health Condition 1: null- localised periodontitis
- Registration Number
- CTRI/2013/09/004013
- Lead Sponsor
- Dr Rameshwari Singhal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
•Subjects of age 18 years or older of either gender in good general health condition
•Subjects with mild to moderate Periodontitis (pocket depth 4-6mm)
•Patients willing to sign Informed Consent Form.
•History of tobacco chewing / smoking
•Any known clinically significant hematological, endocrine disorders, hepatic or renal diseases, cardiovascular, cerebrovascular or psychiatric diseases likely to alter the treatment outcome, or could compromise the subjectâ??s participation in the trial
•Subjects who used medication that would interfere with the efficacy and safety objectives of the trial or who were not stabilized on any concomitant medication (continuous use) during at least three months prior to randomization.
•Patients who participate in other study protocols
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary efficacy outcomes: <br/ ><br>â?¢Gingival index- Loe and Silness <br/ ><br>â?¢Bleeding Index- Ainamo and Bay <br/ ><br>â?¢Plaque Index- Silness and Loe. <br/ ><br>â?¢PPD (Probing Pocket Depth) using Florida probe <br/ ><br>â?¢CAL (clinical attachment level) using Florida probe. <br/ ><br> <br/ ><br>Timepoint: at baseline and 3 months after drug delivery. <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method â?¢Modified OHRQL instrumentTimepoint: Baseline & 3 months