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Clinical Trials/NCT03307798
NCT03307798UnknownNot Applicable

Evaluate a Saw Bone Training Protocol in Using Tactile Sensation to Classify Bone Quality During Implant Surgery

National Taiwan University Hospital1 site in 1 country25 target enrollmentStarted: September 20, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
25
Locations
1
Primary Endpoint
Change on visual analog scale (VAS) score of each test block

Study Overview

Brief Summary

Bone quality is one of the major factors influencing the dental implant survival rate. Bone quality is believed to have effects on initial implant stability and success of osseointegration. Different implant designs and surgical protocols were developed for improving the survival rate in different bone quality. Although bone quality can be partly diagnosed by radiographic images, lots of experienced surgeons also evaluate bone quality with tactile sensation when they drill the bone. However, variations in evaluation of bone density maybe exist among different surgeons. For less experienced dentists, it is difficult to diagnose bone quality with tactile sensation in the beginning. This purpose of this study is to evaluate a training protocol in using tactile sensation to classify bone quality during implant surgery. Saw bones of variant densities are used as training materials. The outcomes before and after training will be compared. The effect of training frequency before surgery will also be evaluated.

Detailed Description

Twenty-five dentists will be enrolled into the study. Tests will be performed using visual analog scale to score bone quality of test blocks.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
26 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Certified dentist with implant surgery experience less than 10 implants.

Exclusion Criteria

  • •Age exceed the limits
  • •Implant surgery experience more or equal to 10 implants

Outcomes

Primary Outcomes

Change on visual analog scale (VAS) score of each test block

Time Frame: 1st time point: test before training & test immediately after training; 2nd time point: 1 week after 1st time point (test after 1 wk); 3rd time point: 1 month after 2nd time point (test after 1month)

Each VAS score performed on the specific test block will be compared between different time point.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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