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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03877419
Other study ID # 201901021RINB
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 28, 2019
Est. completion date January 17, 2020

Study information

Verified date January 2020
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Comparison of different drilling speed to classify bone quality by tactile sensation on a saw bone model


Description:

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. The drilling speed also may have effect on the outcome of evaluation. For less experienced dentists, it is difficult to diagnose bone quality with tactile sensation in the beginning. The purpose of this study is to find proper drilling speed to classify bone quality by tactile sensation on a saw bone model. Saw bones of variant densities are used as training & testing materials. The proper drilling speed to distinguish different bone quality will be evaluated and offered to junior dentists for better implant treatment outcome.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date January 17, 2020
Est. primary completion date December 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 24 Years to 40 Years
Eligibility Inclusion Criteria:

- Adult dentist, with license no more than 5 years

- No clinical implant surgery experience or with experience less than 10 implants.

Exclusion Criteria:

-Subject who couldn't hold the test procedure

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei Test2

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Units on a Visual Analog Score for bone density the range of the visual analog score was from 0 to 100, 0 indicated drilling into the air, 100 indicated drilling into the hardest jaw bone. The investigators will provide participants several saw bone blocks with different density. Participants needed to answer each bone density of blocks on the scale by drilling feedback sensation after drilling. It's better result that the answers close to the correct bone density of the saw bone blocks. 30 minutes
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