The goal of this clinical trial is to learn if the herbal gel is more effective as compared to placebo in reducing periodontal inflammation in patients with periodontal disease. The clinicians shall check various periodontal parameters in the subjects over a scheduled duration. Participants will be administered the gel once subgingivally and the periodontal parameters shall be recorded before gel delivery then again after 1,3 and 6 months. Plaque samples were taken at baseline and 6 months
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Papilla Bleeding Index
Timeframe: 3 months
Plaque Index
Timeframe: 3 months
Probing Pocket Depth
Timeframe: 3 months
Relative Attachment Level
Timeframe: 3 months