CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 4 enrolled
Drug / intervention
Navigated Photogrammetry +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06506747
NCT06506747N/ACompleted

Clinical Evaluation of FastMap Navigated Photogrammetry for Assessing Implant Positions Compared to Standard Stereophotogrammetry

X-Nav Technologies, LLC·observational·Posted Jul 17, 2024·Updated Jun 4, 2025

In Brief

An observational study evaluating Navigated Photogrammetry and Standard Photogrammetry for Doctor Efficiency and Dental Prosthesis Fit. Completed, enrolled 4 participants across 1 site.

Detailed 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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20252026
First PostedJul 17, 2024
Enrollment StartJul 20, 2024
Primary CompletionApr 25, 2025
Study CompletionMay 23, 2025
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 2.0 years ago

Interventions

Navigated Photogrammetrydevice

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.

Standard Photogrammetrydevice

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.