Comparing two types of ultrasonic devices for treating gum disease
Clinical and Patient-Centered Outcomes of Full-Mouth Ultrasonic Debridement for Periodontitis: A Randomized Controlled Trial Comparing Piezoelectric and Magnetostrictive Devices
This study is testing which type of ultrasonic device, piezoelectric or magnetostrictive, works better for treating gum disease and how patients feel about the treatment.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 52 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | University of Siena Academic / other |
| Locations | 1 site (Siena, SI) |
| Trial ID | NCT06934291 on ClinicalTrials.gov |
What this trial studies
This study compares the clinical and psychological outcomes of full-mouth ultrasonic debridement for periodontitis using either piezoelectric or magnetostrictive devices. Patients diagnosed with periodontitis will undergo a thorough periodontal assessment before being randomly assigned to one of the two treatment groups. Following treatment, patient perceptions will be recorded, and a follow-up evaluation will occur three months later to assess the effectiveness of the interventions. The goal is to determine which device yields better outcomes for patients.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old diagnosed with stage 1 or 2 periodontitis and without systemic chronic diseases.
Not a fit: Patients on anticoagulant therapy or who have received antibiotic treatment within three months prior to screening may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment options for patients with periodontitis, enhancing both clinical and psychological outcomes.
How similar studies have performed: Other studies have shown varying success with ultrasonic debridement techniques, but this specific comparison of devices is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * \>18 years * periodontitis of stage 1 and 2 * absence of systemic chronic disease Exclusion Criteria: * anticoagulants treatment * antibiotic treatment 3 months before the screening visit
Where this trial is running
Siena, SI
- Aous — Siena, Si, Italy (Recruiting)
Study contacts
- Study coordinator: Nicola Discepoli, DDS, MSc
- Email: nicola.discepoli2@unisi.it
- Phone: 3395256148
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.