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Clinical Trials/NCT00641277
NCT00641277
Completed
N/A

A Study to Evaluate the Efficacy of the 3mm Maximus Dental Implant in Areas of Limited Tooth-to-tooth Spacing

University of Alabama at Birmingham1 site in 1 country15 target enrollmentMarch 2004
ConditionsEdentulous

Overview

Phase
N/A
Intervention
Not specified
Conditions
Edentulous
Sponsor
University of Alabama at Birmingham
Enrollment
15
Locations
1
Primary Endpoint
peri-implant bone support
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

Dental implants are used in dentistry to reestablish function and appearance to areas of the mouth where natural teeth are missing. Implants can be a good choice for almost all areas of the mouth except where the space left by missing teeth is too narrow. This is usually the case when front teeth are lost of have been missing since birth.

The Maximus dental implant is the smallest implant made, just 3mm in diameter, and is especially designed to replace missing front teeth and yet be strong enough to function as a natural tooth.

This study will assess the functional success of BioHorizons Maximus one-piece endosseous dental implant.

We hypothesize that placement of the 3mm dental implant in areas of limited tooth-to-tooth spacing will be an efficacious tooth root replacement.

Detailed Description

When maxillary anterior (upper front)and/or mandibular incisors are congenitally missing or lost due to other causes, the space between adjacent teeth is frequently too narrow to support traditional implant therapy and patients are often advised to fill the space with conventional fixed or removable prosthetic appliances. The one-piece titanium construction of the Maximus design is believed to retain optimal biomechanical stength while remaining small enough for use in anterior reconstruction thereby allowing access to spaces that were previously beyond the scope of implant dentistry.

Registry
clinicaltrials.gov
Start Date
March 2004
End Date
July 2010
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Michael Reddy, DMD

Dean, School of Dentistry

University of Alabama at Birmingham

Eligibility Criteria

Inclusion Criteria

  • Missing anterior teeth

Exclusion Criteria

  • Pregnancy
  • Cigarette smoking
  • Diabetes Mellitus
  • Other significant medical conditions or habits likely to compromise bone healing
  • Chronic use of medications likely to compromise bone healing

Outcomes

Primary Outcomes

peri-implant bone support

Time Frame: 5 years following prosthetic attachment

Secondary Outcomes

  • Aesthetics and function(5 years following prosthectic attachment)

Study Sites (1)

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