Efficacy of Locally Delivered Tea Tree Oil Gel as an Adjunct to Non-Surgical Periodontal Management
Periodontal Pocket
About this trial
This is an interventional treatment trial for Periodontal Pocket focused on measuring Local Drug Delivery, Periodontitis, Tea Tree Oil
Eligibility Criteria
Inclusion Criteria: Males and females with age range of 25-50years. Patients diagnosed to have (Stage II or Stage III) periodontitis; (3-6 mm CAL, pocket depth ≤ 7 mm, mostly horizontal 15%-33% bone loss as assessed by preoperative radiographs with no tooth loss due to periodontitis). Systemic (medically) free patients. Patients who can follow and maintain oral hygiene instructions. Exclusion Criteria: Pregnant ladies or lactating mothers. Smokers. Patients with history of allergy against one of the components of tea tree oil. Asthmatic patients. Periodontal therapy in the last 6 months
Sites / Locations
- Ain Shams University
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Group I (Test group)
Group II (Control group)
Eleven patients with localized periodontitis, receiving full mouth non-surgical periodontal debridement followed by local delivery of tea tree oil gel as an adjunctive treatment.
Eleven patients with localized periodontitis, receiving full mouth non-surgical periodontal debridement only.