MedTrace Logo

Conventional Versus Digital 3D Printed Complete Removable Dentures

NCT05845099 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2024-09-05

No results posted yet for this study

Summary

The study is a crossover, randomised, controlled clinical trial that will compare and evaluate patients' satisfaction and oral microbiota proliferation in two groups. Group I: Conventionally manufactured CRD Group II: 3D-printed (three-dimensionally printed) CAD/CAM (computer-aided design/computer-aided manufacturing) manufactured CRD, The participants will be selected according to inclusion and exclusion criteria and will be randomly allocated into both groups and then shuffled to the other group using the Research Randomizer Program.

Conditions

  • Denture, Complete

Interventions

DEVICE

Polymethyl Methacrylate-Based Complete Removable Dentures.

The patients will receive Complete Removable Dentures processed by Heat cured acrylic resin.

DEVICE

Photopolymerized Methacrylate- Based Complete Removable Dentures.

The patients will receive a 3D-printed removable denture digitally manufactured using a 3d printer device with light polymerized resin.

Sponsors & Collaborators

  • Ain Shams University

    lead OTHER

Principal Investigators

  • Omnia MS Refai, PHD · lecturer of Oral and Maxillofacial Prosthodontics, Faculty of Dentistry , Ain Shams University

  • Heba RF Elsarrif, PHD · Lecturer of Oral and Maxillofacial Prosthodontics College of oral and dental surgery Misr University for science and technology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
45 Years
Max Age
60 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-12-01
Primary Completion
2024-03-01
Completion
2024-05-01

Countries

  • Egypt

Study Locations

More Related Trials

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 NCT05845099 on ClinicalTrials.gov