Evaluating non-surgical treatments for peri-implantitis
Clinical and Biochemical Evaluation of the Efficacy of Different Non-Surgical Peri-implantitis Treatment Approaches
This study is testing whether a new air abrasion cleaning method or traditional plaque removal works better for treating gum inflammation around dental implants.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Hacettepe University Academic / other |
| Locations | 1 site (Ankara) |
| Trial ID | NCT06849856 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of different non-surgical treatment approaches for peri-implantitis, a common inflammatory condition affecting dental implants. The research focuses on comparing traditional mechanical plaque removal methods using titanium curettes with a novel air abrasion system that utilizes abrasive powder and compressed air for cleaning implant surfaces. The goal is to determine which method provides better long-term clinical outcomes in managing peri-implant diseases. Participants will be monitored for their response to these treatments over a specified period.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-65 with at least one dental implant showing probing depths of 6 mm or deeper and no periodontal treatment in the last 6 months.
Not a fit: Patients with systemic diseases affecting the periodontium, smokers, or those with significant bone loss around their implants may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more effective non-surgical treatments for peri-implantitis, improving patient outcomes and implant longevity.
How similar studies have performed: While traditional methods have shown limited long-term success, the use of air abrasion systems is a novel approach that has not been extensively tested in this context.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Who have not received any periodontal treatment in the last 6 months, 2. Who have not used any medication (antibiotics, anti-inflammatory drugs, antibacterial mouthwashes, corticosteroids) that could affect the results of the study in the last 3 months, 3. Who have at least one implant with a probing depth of 6 mm or deeper in one or more areas in the mouth, and the implant in question has been in function for at least 1 year, 4. Between the ages of 18-65, 5. Individuals who approve the informed consent form will be included in the study. Exclusion Criteria: Individuals who: 1. have a systemic disease that may affect the periodontium, 2. regularly use medication that may affect the periodontium, 3. smoke, 4. are pregnant or lactating, 5. are sensitive to chlorhexidine, 6. have more than 50% bone loss around their current implant(s), 7. do not approve the informed consent form will be excluded from the study.
Where this trial is running
Ankara
- Hacettepe University — Ankara, Turkey (Recruiting)
Study contacts
- Study coordinator: Meltem Ozdemir Kabalak
- Email: dt.meltemozdemir@gmail.com
- Phone: +905377921064
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.