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Clinical Trials/NCT00172718
NCT00172718
Unknown
Not Applicable

Using 3.3mm Screw Tap to Modify the Standard Implantation Procedure and to Measure the Cutting Resistance for Establishing a More Objective Method to Evaluate the Peri-Implant Bone Quality

National Taiwan University Hospital1 site in 1 country60 target enrollmentMarch 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Jaw, Edentulous, Partially
Sponsor
National Taiwan University Hospital
Enrollment
60
Locations
1
Last Updated
17 years ago

Overview

Brief Summary

Osseointegrated root form implants have been applied successfully in treating fully and partially edentulous patients and patients with single tooth missing. However, the success rate of osseointegrated dental implants was not as good in patients with poor bone quality. The reasons are believed that poor bone quality reduces the initial stability of dental implants and then reduces the success rate. For increasing initial stability of dental implants, some technical modifications are suggested in literature. However, due to lack of an objective method to evaluate bone quality, they are controversial. The purposes of this clinical study are to develop a standard procedure which using cutting resistance measured by Osseocare in surgery to evaluate the bone quality and to compare with the clinical experiences of oral surgeons. The objective outcome, initial stability of dental implant, is measured with Osstell. The analyzed results are also helpful for less experienced surgeons.

Detailed Description

Materials \& Methods: 1. Patient eligibility: Six implant surgeons will assist the experiment. The subjects are patient who will receive dental implant treatment in Dental department of NTUH. Sixty subjects are offered by six surgeons. They must fully fill the requirements as following

Registry
clinicaltrials.gov
Start Date
March 2005
End Date
TBD
Last Updated
17 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • No major systemic diseases
  • Mouth opening: \> 35 mm
  • Missing teeth at anterior or premolar area and willing to restored by implantation

Exclusion Criteria

  • Uncomfortable or other condition occurring in the surgical procedure make the measuring unacceptable

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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