Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Recruiting NCT07898332

Comparison of Conventional and Face Scan in Recording the Vertical Dimension of Completely Edentulous Patients

Conditions: Edentulous Complete Denture Wearers

Sex: All
Ages: 55 Years – 75 Years
Healthy volunteers: No
Phase: NA
Enrollment: 18
Sponsor: Ain Shams University

Location: Egyptian Russian University Cairo Nasr City

Summary

The purpose of this study is to evaluate if a 3D face scanner is a reliable and accurate tool for measuring the vertical dimension of occlusion (the optimal height of the lower face) in patients who have lost all their teeth. Currently, dentists determine this measurement manually using clinical judgment, which can sometimes lead to inconsistent results. This study will compare the traditional manual measurement method with a digital face scanning technique. Eighteen completely edentulous (toothless) participants will be enrolled. Each participant will receive two sets of complete dentures: one set fabricated using the new digital face scanning technique and one set fabricated using the traditional method. Researchers will take facial measurements using both a digital caliper directly on the patient's face and a software tool on the 3D scans. The results will help determine if digital scanning is a dependable alternative to conventional methods for improving denture fit, function, and patient comfort.

Eligibility Criteria

Inclusion Criteria:Completely edentulous in both the maxilla and mandible. Willing and able to provide informed consent. Rehabilitated with complete dentures as part of the study protocol. - Exclusion Criteria:Patients suffering from any Temporomandibular Joint Dysfunction (TMD). Patients with any visible facial abnormality. \-

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07898332). StuddyBuddy aggregates publicly available trial information.