NBF Gingival Gel Application After Impacted Lower Third Molar Surgery
Alveolar Osteitis
About this trial
This is an interventional prevention trial for Alveolar Osteitis focused on measuring third molar surgery, oral surgery, propolis, NBF gingival gel, post-surgical complications, clinica trial
Eligibility Criteria
Inclusion Criteria:
The inclusion criteria are:
- cooperative adult patients able to fulfil the study protocol,
- needing surgical extractions of both lower third molars,
- with similar surgical difficulty according to Pederson scale.
Exclusion Criteria:
The exclusion criteria are
- refuse to participate in the study,
- failure to attend 24, 48, and 72 hours, as well as, 7 days post-surgical appointment visits,
- smokers,
- systemic diseases as diabetes mellitus or being immunosuppressed,
- patients who take local or systemic antibiotics less than 3 months ago, anti-inflammatory or anticoagulant medication in the previous 4 weeks,
- patients who require antibiotic prophylaxis,
- pregnant or breastfeeding women,
- patients with chronic periodontitis in active phase or
- with history of allergies to any of the components of local anaesthetics, antibiotics, AINEs, or NBF gingival gel.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
NBF
Placebo
Propolis Extract, Ascorbic Acid, Tocopherol Acetate, Sodium-Monofluorophosphate, Silicon Dioxide, Glycerin, D-sorbitol, Polyethyleneglycol 150, Sodium Carboxymethylcellulose, Xylitol, Sterol Glycoside, Peppermint Oil, L-Menthol, Methyl Hydroxybenzoate and Deionized Water
Sodium-Monofluorophosphate, Silicon Dioxide, Glycerin, D-sorbitol, Polyethyleneglycol 150, Sodium Carboxymethylcellulose, Xylitol, Sterol Glycoside, Peppermint Oil, L-Menthol, Methyl Hydroxybenzoate and Deionized Water