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Digital vs Conventional Prosthetic Rehab & Occlusal Analysis in Edentulous Patients

NCT07164066 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2025-09-09

No results posted yet for this study

Summary

15 Patients requiring complete dentures will be recruited from Dubai Health. Each patient will receive two sets of dentures with a washout period between sets. Patients will remain blinded to the fabrication method used for each set.

* Group 1: Participants will first receive conventionally fabricated dentures for both the upper and lower jaws. This set will be made using traditional techniques, including impressions, a custom tray, jaw relation recording, try-in, and final fitting. After the washout period, they will receive a second set created with the 3D-printed technique.
* Group 2: Participants in this group will initially receive 3D-printed complete dentures through a digital workflow, which involves intraoral scanning, STL file export, digital design, design review with the patient, 3D printing, and final fitting. Following the washout period, they will then receive a conventionally fabricated set.

Conditions

  • Edentulous Complete Denture Wearers
  • Dental Occlusion

Interventions

DEVICE

Digital Occlusal Analysis Device

Computerized occlusal analysis performed using T-Scan and ModJaw devices to record occlusal contacts, timing, and force distribution during prosthesis fitting and function.

Sponsors & Collaborators

  • Mohammed Bin Rashid University of Medicine and Health Sciences

    lead OTHER

Principal Investigators

  • Haitham Elbishari, PhD · MBRU

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-15
Primary Completion
2027-12-31
Completion
2027-12-31

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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 NCT07164066 on ClinicalTrials.gov