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Sonographic Imaging of Oral and Dental Anatomical Structures (A Pilot Study)

Sonographic Imaging of Oral and Dental Anatomical Structures (A Pilot Study)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03657589
Enrollment
20
Registered
2018-09-05
Start date
2017-02-22
Completion date
2018-01-16
Last updated
2018-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alveolar Bone Loss, Gingival Recession, Oral Mucosa, Ultrasound

Brief summary

The overall purpose of this study is to establish an ultrasound technique to aid in oral and dental examination of soft and hard tissues. Ultrasound is currently not used in Dentistry and associated oral examinations and its usefulness for clinical practice will be explored. This study will investigate the use of ultrasonic imaging for planning and placing dental implants, as well as evaluate the use of ultrasonic imaging for monitoring marginal bone loss around dental implants.

Detailed description

This study will involve two different groups of subjects: Patients scheduled for a dental implant procedure, and patients scheduled for a revision surgery after developing infection after implant surgery. Twenty subjects examining only specific aim one is funded and will be studied. If future funding is granted and additional 30 subjects for aim one and 40 for aim two will be studied Subjects in both groups will receive an ultrasound examination of the oral cavity prior to their clinically-scheduled dental surgery. Subjects in group 1 also may receive a CBCT scan if not previously clinically-ordered.

Interventions

None listed

Sponsors

MICHR Pilot grant (UL1TR000433)
CollaboratorUNKNOWN
Delta Dental Foundation
CollaboratorOTHER
POM Supplemental Grant
CollaboratorUNKNOWN
SOD Collision Award
CollaboratorUNKNOWN
AAP's SUNSTAR Innovation Grant
CollaboratorOTHER
University of Michigan
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
Yes

Inclusion criteria

* Subjects 18 years of age and older who will be scheduled to have an implant surgery from premolar to premolar with bilateral adjacent teeth present will be recruited.

Exclusion criteria

* Patients under 18 years of age. * Unwilling or unable to read and sign this informed consent document. * Do not have a tooth on each side of the implant that will be placed. * Women who are pregnant or unsure of their pregnancy status.

Design outcomes

Primary

MeasureTime frameDescription
ultrasound soft tissue thicknessAt least 6 months after implant crown placement (1 time point)soft tissue thickness at the missing tooth gap and adjacent teeth were measured with ultrasound

Secondary

MeasureTime frameDescription
ultrasound alveolar bone heightAt least 6 months after implant crown placement (1 time point)alveolar bone height at the missing tooth gap and adjacent teeth was measured

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026