MedTrace Logo

Multicenter Retrospective Study Evaluating ATLANTIS™ Abutment Teeth Connected to Implants

NCT02496091 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 144

Last updated 2020-04-28

Study results available
· View outcomes & findings →

Summary

The study is designed as a retrospective and multi-center study. The study population is US individuals previously restored with titanium and gold-shaded titanium ATLANTIS abutments. The study includes retrospective data collection from the medical records and data collection from one prospective study visit with a clinical examination.The primary objective is to evaluate success. Success is defined as that the study implant and abutment are in situ and no Adverse Device Effects related to the study implant, abutment or adjacent peri-implant tissues are reported during the study.

Conditions

  • Dental Implants

Interventions

DEVICE

ATLANTIS Abutment

Sponsors & Collaborators

  • Dentsply Sirona Implants and Consumables

    lead INDUSTRY

Principal Investigators

  • Dr Ingeborg J. Dr De Kok, DDS · University of North Carolina, School of Dentistry, Chapel Hill, NC 27599, US

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-08-31
Primary Completion
2018-03-30
Completion
2018-03-30

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02496091 on ClinicalTrials.gov