Evaluating the timing of follow-up after non-surgical periodontal therapy
Timing of Re-evaluation After Steps I-II of Periodontal Therapy: a Randomized Clinical Trial
This study is testing how different follow-up times after non-surgical gum treatment can affect healing and costs for people with gum disease.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Turin, Italy Academic / other |
| Locations | 1 site (Turin) |
| Trial ID | NCT05892315 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the optimal timing for re-evaluation after non-surgical periodontal therapy (NSPT) in patients with periodontitis. It aims to determine how different re-evaluation intervals of 1, 3, and 6 months affect clinical outcomes such as pocket closure and probing pocket depth reduction. The study will also assess the impact of these timings on the overall treatment plan and associated costs for patients. Participants will undergo repeated subgingival instrumentation and supragingival scaling as part of their treatment.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older with stage III-IV periodontitis who meet specific clinical criteria.
Not a fit: Patients under 18, pregnant or lactating women, heavy smokers, and those with conditions affecting periodontal healing may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment protocols for periodontitis, enhancing patient outcomes and reducing costs.
How similar studies have performed: While there is limited clarity in existing literature regarding re-evaluation timing in NSPT, this study aims to fill a gap, making it a novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Periodontitis stage III-IV * Full-mouth plaque score (FMPS) \< 25% at the 1-month re-evaluation * Full-mouth bleeding score (FMBS) \< 25% at the 1-month re-evaluation * Signed informed consent Exclusion criteria: * Age \< 18 yo * Pregnancy or lactation * Heavy smokers (\>10 die) * Conditions or diseases influencing periodontal healing * Patients that cannot complete the 6 months follow-up
Where this trial is running
Turin
- CIR Dental School — Turin, Italy (Recruiting)
Study contacts
- Study coordinator: Mario Aimetti, Professor
- Email: mario.aimetti@unito.it
- Phone: 00390116331541
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.