Multicenter Clinical Randomized Controlled Trial Evaluation of an Implant System Designed for Enhanced Primary Stability.
Clark M Stanford, Chris Barwacz, Stephanie Raes...
https://pubmed.ncbi.nlm.nih.gov/27447160Actively Recruiting
Age: 18Years - 99Years
All Genders
ID05500755
Clinical and Radiographic Evaluation of Dentsply Sirona PrimeTaper Implants: A Prospective Medium Term Study
Led by Aula Dental Avanzada · Updated on 2025-08-19
150
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the clinical and radiographic performance of the DS PrimeTaper dental implant system, recently introduced by Dentsply Sirona. This implant has design changes from its predecessor, including variable thread forms and a more aggressive taper to improve cutting ability. The study aims to provide medium-term clinical data to guide clinicians before the usual 10- to 15-year follow-up periods are available. Participants will receive surgical placement of at least one DS PrimeTaper implant followed by its prosthetic restoration. This observational study focuses on patients treated with this dental implant system to collect real-world clinical outcomes and complications over about one year. During the study, researchers will monitor implant survival and success rates and record any biological or mechanical complication events. The evaluation includes clinical and radiographic assessments, with data collected through the completion of the study, averaging one year. The study began in 2022 and is expected to continue until the end of 2026.
CONDITIONS
Brief Title
Clinical and Radiographic Evaluation of Dentsply Sirona PrimeTaper Implants
Who Can Participate
Age: 18Years - 99Years
All Genders
Eligibility Criteria
You may qualify if you...
- Patients who have received at least one DS Prime Taper implant
You will not qualify if you...
- Dental implant surgery is contraindicated for the patient
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
1
2
3
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Implementation
Duration - Day of surgery
Participants undergo surgical placement of a DS Prime Taper implant and its posterior prosthesis.
1 visit (in-person)
Post-operative Follow-up
Duration - Up to 1 year
Participants are monitored for implant survival, success, and biological or mechanical complications over approximately 1 year.
Regular follow-up visits over 1 year
Trial Site Locations
Total: 1 location
1
Clínica Dental esteve
Alicante, Alicante, Spain, 03001
Actively Recruiting
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Research Team
G
Guillem Esteve-Pardo, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Published Research Related To This Trial
Improvement in Fatigue Behavior of Dental Implant Fixtures by Changing Internal Connection Design: An In Vitro Pilot Study.
Nak-Hyun Choi, Hyung-In Yoon, Tae-Hyung Kim...
https://pubmed.ncbi.nlm.nih.gov/31591290Clinical Evidence of OsseoSpeed EV Implants: A Retrospective Study and Characterization of the Newly Introduced System.
Marco Toia, Silvia Galli, Denis Cecchinato...
https://pubmed.ncbi.nlm.nih.gov/28834532