Dental Implant Stability When Using the Densah Bur™ Bone Compaction Process to Prepare Dental Implant Sites

Withdrawn before enrolling

Conditions studied: Missing Teeth

In brief

The primary objective of this study is to determine if the use of a bone compaction process (osseodensification) (Densah™ bur: Versah Osseodensification Company™) to prepare dental implant sites, in human subjects, results in increased bone-ridge width, increased compact bone in the outer wall of the prepared sites, and dental implant stability.

Key facts

Study ID

NCT02502058

Run by

University of Minnesota

People needed

0

Starts

2015-07-01

Expected to finish

2017-03-01

Last updated by the study team

2017-06-20

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Males and females
• Ages 18-80 years of age
• Missing at least one tooth.
• Capable of giving informed consent

You may not qualify if…

• Patient is a pregnant female
• Patient smoking more than 5 cigarettes per day
• Patient has a history of alcoholism or drug abuse during the last 5 years
• Patient with uncontrolled hypertension or diabetes
• Patient has a malignant tumor
• Patient is on daily dose of steroids
• Patient with history of chemotherapy or radiation for the last 12 months
• Patient who is immuno suppressed
• Patient with titanium allergy
• Subject should not be a homeless person

Where it is running

• Oral Health Research Clinic at the School of Dentistry at the University of Minnesota — Minneapolis, Minnesota, United States

Full record on ClinicalTrials.gov

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