Overview

This trial is active, not recruiting.

Conditions partial edentulism, tooth disease
Sponsor Biomet, Inc.
Start date January 2011
End date December 2016
Trial size 47 participants
Trial identifier NCT01529762, 3007

Summary

Osseotite Certain Tapered implants placed in immediate prosthesis loaded cases.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Observational model cohort
Time perspective prospective
Arm
Dental implant Osseotite Certain Tapered design

Primary Outcomes

Measure
cumulative success rate
time frame: 3 years

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: - patients of either sex and older than 18 years of age - patients needing at least one dental implant to treat partial edentulism - patients physically able to tolerate surgical and restorative dental procedures - patients agreeing to all protocol visits Exclusion Criteria: - patients with infection or severe inflammation at the intended treatment sites - patients smoking greater than 10 cigarettes per day - patients with uncontrolled diabetes mellitus - patients with uncontrolled metabolic diseases - patients who received radiation treatment to the head in the past 12 months - patients needing bone grafting at the intended treatment sites - patients known to be pregnant at screening visit - patients with para-functional habits like bruxing and clenching

Additional Information

Official title A Prospective, Observational Study of Immediate Loading Cases Using Osseotite Certain Tapered Implants
Principal investigator Fernando Fuentes, DDS
Description Osseotite Certain Tapered implants are placed and restored immediately (during the same visit)
Trial information was received from ClinicalTrials.gov and was last updated in March 2016.
Information provided to ClinicalTrials.gov by Biomet, Inc..