A modified technique for sinus floor elevation in patients with limited bone height
A Modified Sinus Floor Elevation Technique - a Pilot Study on 12 Patients
This study tests a new, less invasive surgery for people with low bone height to see if it can create enough space for dental implants while also making the experience less stressful for patients.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 12 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | All |
| Sponsor | Medical University of Vienna Academic / other |
| Locations | 1 site (Vienna) |
| Trial ID | NCT02137824 on ClinicalTrials.gov |
What this trial studies
This pilot study aims to evaluate a modified minimally invasive surgical technique for sinus floor augmentation in patients with a residual bone height of 3-6mm. The investigators hypothesize that this technique will create an adequate implant bed of at least 10mm height after a healing period of 3-5 months, while also reducing patient stress levels. The study will involve 12 patients undergoing sinus floor elevation procedures to assess the effectiveness and safety of the approach.
Who should consider this trial
Good fit: Ideal candidates for this study are patients with a residual bone height of 3-6mm and a residual bone width greater than 4mm.
Not a fit: Patients with untreated periodontal disease, smokers, or those suffering from acute or chronic sinusitis may not benefit from this study.
Why it matters
Potential benefit: If successful, this technique could provide patients with a less invasive option for sinus floor augmentation, improving their chances of successful dental implant placement.
How similar studies have performed: While this approach is innovative, similar minimally invasive techniques have shown promise in other studies, suggesting potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * residual bone height of 3-6mm * residual bone width of \>4mm Exclusion Criteria: * not treated periodontal disease * smoker (\>5cig/day) * acute or chronic sinusitis
Where this trial is running
Vienna
- Bernhard Gottlieb School of Dentistry, Medical University of Vienna — Vienna, Austria (Recruiting)
Study contacts
- Study coordinator: Kristina Bertl, PD, DMD, MSc
- Email: kristina.bertl@meduniwien.ac.at
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.