Improving recovery after dental implants using vibropneumostimulation
Clinical and Functional Rationalization of the Use of Vibropneumostimulation in the Rehabilitation System of Patients After Dental Implantation
This study is testing a new technique using special vibrations to help people recover better after getting dental implants.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Sex | All |
| Sponsor | Samara State Medical University Academic / other |
| Locations | 1 site (Samara) |
| Trial ID | NCT05758337 on ClinicalTrials.gov |
What this trial studies
This study aims to enhance the rehabilitation process for patients undergoing dental implantation by utilizing a novel technique involving vibropneumostimulation. The approach includes the use of a specialized dental implant made from non-woven titanium and a unique vibropneumostimulator designed to activate bone remodeling. Various functional and clinical methods, such as thermography and radiography, will be employed to assess the effectiveness of this treatment. The goal is to improve both the functional and anatomical outcomes for patients post-implantation.
Who should consider this trial
Good fit: Ideal candidates for this study include patients with a history of unsuccessful dental implantations, low bone density, or those who have undergone sinus lifting surgery.
Not a fit: Patients without a history of dental implant issues or those with normal bone density may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to improved healing and integration of dental implants, resulting in better patient outcomes.
How similar studies have performed: While this specific approach is novel, similar studies exploring the effects of mechanical stimulation on bone healing have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients with a history of previous unsuccessful implantations, * patients with a history of bad habits, * patients with low bone density (CT), * patients who have sinus lifting surgery performed simultaneously Exclusion Criteria: No \-
Where this trial is running
Samara
- Samara state medical university — Samara, Russia (Recruiting)
Study contacts
- Study coordinator: Ivan Bayrikov, MD
- Email: i.m.bajrikov@samsmu.ru
- Phone: +79061274992
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.