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Clinical Trial Summary

This will be a prospective, randomized multicenter study to determine the safety and efficacy of the T3 Certain Tapered with DCD as compared to T3 Certain Tapered without DCD. All implants will be placed in the maxilla or mandible in a single stage manner and loaded with prosthesis after 6 weeks of healing. Final restorations will take place no later than 4 months following implant placement surgery. The implants will be evaluated yearly for 2 years.


Clinical Trial Description

This is a multicenter, prospective, randomized study that will assess the the safety and efficacy of the implant systems with: - Resistance to countertorque testing (mobility) - Implant Stability Quotient (ISQ) - Changes in peri-implant crestal bone levels - Confirmation of clinical benefits A total of 60 implants, 30 per treatment group will be placed across all participating sites. One patient may contribute more than 1 implant. All implants/ patients will be followed for up to 2 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04354688
Study type Interventional
Source ZimVie
Contact
Status Active, not recruiting
Phase N/A
Start date October 19, 2019
Completion date July 2024

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