Evaluation of EUROTEKNIKA Dental Implants for Missing Teeth
Real-life Evaluation of the Safety and Performance of EUROTEKNIKA Dental Implants
This study is testing how safe and effective EUROTEKNIKA dental implants are for people with missing teeth to see how they improve smiles and overall oral health.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 868 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Euroteknika Industry-sponsored |
| Locations | 1 site (Clermont-Ferrand) |
| Trial ID | NCT05375045 on ClinicalTrials.gov |
What this trial studies
This study evaluates the safety and performance of EUROTEKNIKA dental implants in real-life settings for patients with missing teeth. It focuses on individuals who are partially or completely edentulous and assesses the impact of these implants on aesthetic, functional, and psychological aspects of oral health. The study includes both a prospective cohort of patients receiving new implants and a retrospective cohort of patients who received implants before 2017. The implants are made of titanium or titanium alloy and are designed to support dental prostheses.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18 and over who are partially or totally edentulous and are undergoing implantation with EUROTEKNIKA dental implants.
Not a fit: Patients who are pregnant, breastfeeding, or have contraindications to dental implantation may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve the quality of life for patients with missing teeth by restoring their masticatory function and enhancing their aesthetic appearance.
How similar studies have performed: Previous studies on dental implants have shown positive outcomes, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient aged 18 or over * Patient who has completed bone growth * Patient informed and agreeing to participate in the study * Partially or totally edentulous patient who will be implanted with the EUROTEKNIKA dental implant (for the prospective cohort) * Patient to benefit from the placement of an implant for the creation of a single crown (for the prospective cohort) * Patient implanted with the EUROTEKNIKA dental implant before 2017 (for the retrospective cohort) * Patient having benefited from the placement of an implant for the creation of a single crown (for the retrospective cohort) Exclusion Criteria: * Pregnant or breastfeeding women (for the prospective cohort) * Patient with bone disease in the cervico-facial region * Patient refusing to participate in the study * Patient with at least one contraindication to implantation (for the prospective cohort) * Patient to benefit from the placement of an implant with immediate or early loading (for the prospective cohort) * Patient to benefit from the placement of an implant for the support of the bridge, piles, attachment (for the prospective cohort) * Patient having benefited from the placement of an implant with immediate or early loading (for the retrospective cohort) * Patient having benefited from the placement of an implant for the support of the bridge, piles, attachment (for the retrospective cohort)
Where this trial is running
Clermont-Ferrand
- Chu Clermont Ferrand — Clermont-Ferrand, France (Recruiting)
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.