Registry for Z-Systems Z5m Dental Implants
Post Market Clinical FoIIow up (PMCF) Medical Device (MD) of Z-Systems Monotype Zirconia Dental Product: Z5m Dental Implants Registry
This study is looking at how well Z-Systems Z5m dental implants made from a special ceramic material work for adults who have had or will get these implants, especially for those who prefer a metal-free option.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 70 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Z-Systems Industry-sponsored |
| Locations | 1 site (Olten) |
| Trial ID | NCT06007365 on ClinicalTrials.gov |
What this trial studies
This observational study aims to collect data on the performance and outcomes of Z-Systems Z5m dental implants, which are made from zirconia, a biocompatible ceramic material. The study will involve adult patients who have received or will receive up to five of these implants, focusing on their experiences and the implants' effectiveness. By gathering this information, the study seeks to provide insights into the viability of zirconia implants as a metal-free alternative in dentistry, particularly for patients with aesthetic concerns.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are receiving Z-Systems Z5m dental implants.
Not a fit: Patients who are unable to provide informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide evidence supporting the use of zirconia dental implants as a safe and effective alternative to traditional titanium implants.
How similar studies have performed: While there is a growing body of literature on zirconia implants, this specific registry approach for Z-Systems Z5m implants is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patient (≥ 18 years) was or will be implanted with up to 5 implants of the Z-Systems Z5m product group * Patient has signed Informed Consent. Exclusion Criteria: • Inability to give consent
Where this trial is running
Olten
- Praxis am Klosterplatz — Olten, Switzerland (Recruiting)
Study contacts
- Study coordinator: Nutcha Bürki, PhD
- Email: clinical@zsystems.com
- Phone: +41 62 531 69 09
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.