Comparing treatments for gum inflammation around dental implants
Impact of Non-surgical Treatment of Peri-implant Mucositis on Incongruous Dental Prostheses Versus Congruous on a Single Tooth Restoration
NA · University of Catania · NCT05923554
This study tests whether a specific gum treatment works better for people with different types of dental implants to reduce inflammation and bleeding around them.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 56 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | University of Catania (other) |
| Locations | 1 site (Catania) |
| Trial ID | NCT05923554 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of non-surgical periodontal therapy in resolving peri-implant mucositis by comparing patients with congruous and non-congruous single dental implant restorations. Participants will undergo treatment to assess changes in probing depth and clinical improvement. The study focuses on patients exhibiting bleeding in the subgingival space, with the goal of determining which type of dental restoration yields better outcomes in managing gum inflammation.
Who should consider this trial
Good fit: Ideal candidates are individuals with peri-implant mucositis who have bleeding on probing and no history of periodontal disease or systemic diseases.
Not a fit: Patients with existing periodontal disease or systemic conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment protocols for patients with peri-implant mucositis, enhancing their oral health and implant longevity.
How similar studies have performed: While the specific comparison of congruous versus non-congruous restorations is novel, similar studies on non-surgical treatments for peri-implant mucositis have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * peri-implant mucositis * bleeding on probing and/or a gingival index \<1 at least at one site at baseline * absence of peri-implant bone loss during the last 2 years before baseline Exclusion Criteria: * Periodontal disease * Systemic diseases
Where this trial is running
Catania
- AOU Policlinico G. Rodolico — Catania, Italy (RECRUITING)
Study contacts
- Principal investigator: Gaetano Isola — Università degli Studi di Catania
- Study coordinator: Gaetano Isola
- Email: gaetano.isola@unict.it
- Phone: 0953785652
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.
Conditions: Bleeding of Subgingival Space