Skip to content

Lidar-based Scanning of Fascial Edema (FE)

Handheld vs Mechanically-assisted Scanning of Fascial Edema Following Impacted Third Molar Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07690488
Acronym
FE
Enrollment
20
Registered
2026-07-08
Start date
2025-12-01
Completion date
2026-06-03
Last updated
2026-07-08

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

Conditions

Edema Face, Scanning Devices

Keywords

Fascial edema, Lidar-based scanning, mobile device, mechanically assisted, handheld, flexible ruler

Brief summary

This study compared handheld and mechanically assisted scanning to evaluate fascial edema after third molar extraction. The flexible ruler served as the reference. Linear measurements were taken from the tragus to the pogonion, from the tragus to the corner of the mouth, and from the lateral corner of the eye to the angle of the mandible.

Detailed description

This study compared Lidar-based scanning methods for evaluating fascial edema after third molar extraction. The three methods assessed were flexible ruler measurement, handheld scanning, and mechanically assisted scanning. Lidar-based scanning was performed using a mobile device and a dedicated application. Linear measurements were obtained from the tragus to the pogonion, from the tragus to the corner of the mouth, and from the lateral canthus to the angle of the mandible. The study objectives were to compare scanning methods, evaluate acquisition time and the number of repeated scans required for mobile scanning, and assess patient-related outcomes using a questionnaire.

Interventions

PROCEDUREMeasurement with flexible ruler

linear measurements were obtained directly using a flexible ruler marked in millimeters

PROCEDUREMeasurement with handheld scanning

Face image of patients were collected using a LiDAR-equipped mobile device and the three dimensional scanning application. A researcher was manually moved around the participant's head along a horizontal trajectory until complete facial coverage and adequate mesh reconstruction.

PROCEDUREMeasurement with mechanically assisted scanning

Face image of patients were collected using a LiDAR-equipped mobile device and the three dimensional scanning application. For recording, the device is positioned on a mechanism.

Sponsors

Ege University
Lead SponsorOTHER
The Scientific and Technological Research Council of Turkey
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Presence of at least one impacted mandibular third molar, * Complete root development of the impacted tooth, * Impaction classified as Pell and Gregory Level B and Winter Class II (vertical position)

Exclusion criteria

* Pregnancy or lactation; * Neurological, endocrine, or psychiatric disorders associated with tremor or hereditary disorders affecting motor function, * Facial asymmetry, facial deformity, or facial hair that could interfere with facial contour assessment; * Current or planned use of medications that may influence postoperative facial edema, such as corticosteroids; * Presence of chronic conditions that could mimic facial edema or a history of complications such as hematoma or subcutaneous emphysema.

Design outcomes

Primary

MeasureTime frameDescription
Collect fascial anthropometric measurementAt postoperative first weekThe measurement of the distances between the tragus and pogonion, the tragus and labial commissure, and the angle of mandible and lateral canthus with the use of a flexible ruler, handheld scanning, and mechanically assisted scanning.

Secondary

MeasureTime frameDescription
Collect of image acquisition timeAt postoperative first weekThe duration required to complete facial recordings using both handheld scanning and mechanically assisted scanning.
Collect of the number of repeated scansAt postoperative first weekRequired repetitions for capturing facial recordings using handheld scanning or mechanically assisted scanning.
Collect of patient reported outcomesAt postoperative 7th dayA questionnaire was used to assess patient's perception to measurement methods

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 9, 2026