Actively Recruiting
Real-life Evaluation of the Safety and Performance of EUROTEKNIKA Dental Implants
Led by Euroteknika · Updated on 2022-05-16
868
Participants Needed
1
Research Sites
305 weeks
Total Duration
On this page
Sponsors
E
Euroteknika
Lead Sponsor
E
EVAMED
Collaborating Sponsor
AI-Summary
What this Trial Is About
Real-life evaluation of the safety and performance of EUROTEKNIKA dental implants
CONDITIONS
Official Title
Real-life Evaluation of the Safety and Performance of EUROTEKNIKA Dental Implants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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)
You will not qualify if you...
- 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)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Chu Clermont Ferrand
Clermont-Ferrand, France, 63003
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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