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Navigated Photogrammetry Compared to Standard Stereophotogrammetry

NCT06506747 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4

Last updated 2025-06-04

No results posted yet for this study

Summary

The purpose of this study is to compare the clinical outcome of Navigated Photogrammetry to standard stereophotogrammetry techniques in digital dentistry for the following two parameters:

* The amount of time needed to prepare the provisional digital files for use in the lab, measured in direct doctor interaction time.
* Suitability of delivered provisional occlusion.

Participants will receive either a provisional manufactured by the output of Navigated Photogrammetry, or a provisional manufactured by the output of standard stereophotogrammetry.

Conditions

  • Doctor Efficiency
  • Dental Prosthesis Fit

Interventions

DEVICE

Navigated Photogrammetry

Navigated Photogrammetry shall be performed following implant surgery, rather than standard stereophotogrammetry. The patient will then receive a provisional that was manufactured using the data from FastMap Navigated Photogrammetry.

DEVICE

Standard Photogrammetry

The patient will receive the existing patient care protocol that includes anatomy information for the manufacturing of the provisional. Specifically, the patient will receive a preoperative IntraOral Scan (IOS) anatomy scan with IOS-compatible fiducials. Following implant surgery, the patient will receive a scan with a standard stereophotogrammetry device. Additionally, they will receive a post-op alignment IOS with IOS-compatible anatomy fiducials and IOS-compatible implant scan bodies. The patient will then receive a provisional that was manufactured using the data from the standard stereophotogrammetry device.

Sponsors & Collaborators

  • X-Nav Technologies, LLC

    lead INDUSTRY

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-07-20
Primary Completion
2025-04-25
Completion
2025-05-23
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06506747 on ClinicalTrials.gov