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Ultrasonography and Cone-Beam Computed Tomography for Peri-implant Tissue Evaluation

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University of Michigan

Status

Completed

Conditions

Ultrasonography

Study type

Observational

Funder types

Other

Identifiers

NCT04488302
HUM00179671

Details and patient eligibility

About

Objectives: Although cone-beam computed tomography (CBCT) is becoming a standard of care in implant therapy, concerns have been raised recently about its limitation in imaging peri-implant tissues due to artifacts. The aim of present study was to demonstrate the complementary role of ultrasound (US), for a comprehensive examination of peri-implant tissues in live humans. Material and Methods: Patients with > 1 implant, a CBCT scan, an US scan, and clinical photographs taken during the open-bone surgery were included. The crestal bone thickness (CBT) and facial bone level (FBL) were measured on both modalities, and direct FBL measurements were also made on clinical images. The correlation plots were made to evaluate the measurement agreements between the 3 methods.

Enrollment

4 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • the patients had to have ≥ 1 implant with a CBCT scan, US scan, and clinical photographs taken during the surgery, e.g. a revision/explantation surgery due to peri-implantitis or a 2nd stage uncover surgery.

Trial design

4 participants in 1 patient group

Implant group
Description:
Patients with 1 or more implants with CBCT, ultrasound and open-bone images

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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