Treatment of deep periodontal pockets using a special device and erythritol powder
Evaluation Of Nonsurgical Treatment Of Deep Periodontal Pockets (7-10mm) Using AIRFLOW® Prophylaxis Master Device With Erythritol Powder vs Conventional Instrumentation: A Randomized Controlled Clinical Trial
This study is testing whether a special device using erythritol powder can better treat deep gum pockets in people with gum disease compared to regular cleaning methods.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 46 (estimated) |
| Ages | 16 Years to 80 Years |
| Sex | All |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06490679 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of the AIRFLOW® Prophylaxis Master Device with erythritol powder compared to conventional instrumentation for treating deep periodontal pockets (7-10mm) in patients with periodontitis. Patients will undergo a thorough clinical examination and periodontal charting, followed by treatment that includes biofilm removal using the AIRFLOW® device. The study aims to assess clinical outcomes through various measurements, including probing depth and clinical attachment level, over a period of six months. Participants will be recruited from the outpatient clinic of the Oral Medicine and Periodontology Department at Cairo University.
Who should consider this trial
Good fit: Ideal candidates include systemically healthy individuals aged 16 to 80 with periodontitis and at least one deep periodontal pocket measuring 7 to 10 mm.
Not a fit: Patients with systemic conditions such as diabetes, pregnant or lactating females, and those with severe respiratory infections or inflammation may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could provide a more effective and less invasive option for managing deep periodontal pockets, potentially improving oral health and reducing tooth loss.
How similar studies have performed: While the use of air abrasive devices in periodontal treatment has been explored, this specific approach with erythritol powder is relatively novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Systemically healthy patients. * Patients with an age range between 16 to 80 years. * Patients have a minimum of 20 teeth. * Periodontitis patients with at least one residual pocket with a probing depth ranging from 7 to 10 mm. * Cooperative patients able and willing to come for follow up appointments. Exclusion Criteria: * Pregnant and lactation females. * Patients reporting systemic conditions (eg: diabetes). * Patients with severe or unstable upper respiratory tract infections, chronic bronchitis/asthma. * Patients with severe inflammation and/or osteonecrosis.
Where this trial is running
Cairo
- Faculty of Dentistry, Cairo University — Cairo, Egypt (Recruiting)
Study contacts
- Principal investigator: Mohammad Aldawod, Bachelor — Cairo University
- Study coordinator: Mohammad Aldawod, Bachelor
- Email: mohammad.alaa@dentistry.cu.edu.eg
- Phone: 00201065747906
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.