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CompletedNCT07091552

Clinical Assessment of CAD/CAM Monolithic Complete Denture

Clinical Assessment of CAD/CAM Monolithic Complete Denture (Cross Over Controlled Clinical Trial)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
22 (actual)
Sponsor
Eman Assam · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The aim of the study is to evaluate trueness, tooth position, retention, and patient satisfaction of CAD/CAM monolithic complete denture

Conditions

Interventions

TypeNameDescription
DEVICECAD/CAM monolithic dentureBased on the workflow suggested by the Ivoclar digital denture, conventional complete dentures will be scanned by using desktop scanner (Medit T710). The cameo and intaglio surfaces of the complete dentures will be scanned, and the scanned data will be exported as Standard Tessellation Language (STL) file to start the milling process. For the milling process, monolithic denture will be milled from a bicolored disk (Ivotion). One side is the denture base material made of high impact optimized polymethyl methacrylate (PMMA) while the other is the teeth material made of highly cross-linked PMMA with no filler. The bicolor disk is milled in a 5-axis milling machine in wet condition, through an uninterrupted milling process. Following the fast milling process the dentures will be finished and polished.
DEVICEConventional dentureThe conventional set will be fabricated with the 5-appointment process: preliminary impressions (first appointment); definitive impressions (second appointment); interocclusal records and tooth selection (third appointment), the size of the teeth will be selected according to the library provided by 3Shape Dental System software to match the disc size; wax trial placement (fourth appointment); and denture adjustment and placement (fifth appointment). Conventional CD will be fabricated with the conventional lost wax technique and heat-polymerizing acrylic resin. The heat-polymerized CDs will be finished, and polished before placement. Adjustments will be made for the polished surface, tissue surface, borders, and occlusion. Occlusal errors will be adjusted through clinical remount of the finished dentures.

Timeline

Start date
2024-01-12
Primary completion
2025-04-05
Completion
2025-04-05
First posted
2025-07-29
Last updated
2025-07-29

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07091552. Inclusion in this directory is not an endorsement.