The Use of Adhesion Molecule Loaded Hydrogel With Minimally Invasive Surgical Technique in Treatment of Periodontal Intrabony Defect
Periodontitis
About this trial
This is an interventional treatment trial for Periodontitis focused on measuring adhesion molecule, intrabony defect, hydrogel, Minimally invasive surgical technique
Eligibility Criteria
Inclusion Criteria: - Patients with diagnosis of periodontitis (stage III or IV and grade B or C) according to new American Academy of Periodontology classification (Tonetti et al., 2018a) (Nguyen et al., 2021). Selected patients of both sexes were 20-55 years old. All single and multiple rooted teeth in both maxilla and mandible. Presence of interdental periodontal pocket with intrabony defect. Patients were free from any systemic diseases that could alter their periodontal status, complicate the surgical treatment, or affect healing according to Modified Cornell Index (Abramson, 1966). No antibiotics or any medications that affect bone or soft tissue condition were taken during the last six months. Exclusion Criteria: Patients who received regenerative periodontal therapy last 6 months before the initial examination. Pregnant or lactating females. Smokers were not included as participants in this study. Patients not committed to oral hygiene after the re-evaluation of phase I therapy. Teeth with mobility more than Grade I. Third molars.
Sites / Locations
- Shaimaa Hamdy
- Shaimaa Hamdy
Arms of the Study
Arm 1
Arm 2
Arm 3
Placebo Comparator
Placebo Comparator
Active Comparator
Group 1
Group 2
Group 3
Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with modified minimally invasive surgical technique (M-MIST) alone
Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with (M-MIST) and hydrogel injection
Fifteen periodontitis patients will receive Phase I therapy, reevaluation after four weeks with (M-MIST) and RGD peptide hydrogel.