Skip to main content
OpenTrials
Completed

NCT Number: NCT07690488

Lidar-based Scanning of Fascial Edema (FE)

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Ege University

Izmir, Bornova, 35550, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Measurement with flexible ruler

Procedure

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

Measurement with handheld scanning

Procedure

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.

Measurement with mechanically assisted scanning

Procedure

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.

Primary outcomes

  1. Collect fascial anthropometric measurement

    Time frame: At postoperative first week

    The 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 outcomes

  1. Collect of image acquisition time

    Time frame: At postoperative first week

    The duration required to complete facial recordings using both handheld scanning and mechanically assisted scanning.

  2. Collect of the number of repeated scans

    Time frame: At postoperative first week

    Required repetitions for capturing facial recordings using handheld scanning or mechanically assisted scanning.

  3. Collect of patient reported outcomes

    Time frame: At postoperative 7th day

    A questionnaire was used to assess patient's perception to measurement methods

Sponsors and collaborators

Lead sponsor

Ege University

Other

Collaborators

  • The Scientific and Technological Research Council of Turkey

Registry information

Official study title

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

Acronym: FE

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jul 8, 2026
Registry last updated
Jul 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.