Actively Recruiting
"Patient Satisfaction with Intra-Oral Vs. Extra-Oral Scanned 3D-Printed Dentures: an in Vivo Study"
Led by Cairo University · Updated on 2025-02-26
8
Participants Needed
1
Research Sites
91 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to evaluate patient satisfaction with intra-orally scanned versus extra-orally scanned digitally printed maxillary dentures in completely edentulous patients. The main questions it aims to answer are: 1. Do intra-orally scanned dentures provide higher patient satisfaction compared to extra-orally scanned dentures? 2. Are there significant differences in comfort, fit, aesthetics and phonetics between the two types of dentures? Researchers will compare the intra-orally scanned denture group to the extra-orally scanned denture group to determine if one method leads to superior patient-reported outcomes. Participants will: * Receive both types of dentures (intra-orally scanned and extra-orally scanned), with a three-week wash-out period between each intervention. * Complete satisfaction surveys to assess comfort, fit, and aesthetics after using each type of denture. The study aims to provide evidence on the optimal scanning method for digitally printed maxillary dentures in edentulous patients.
CONDITIONS
Official Title
"Patient Satisfaction with Intra-Oral Vs. Extra-Oral Scanned 3D-Printed Dentures: an in Vivo Study"
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Completely edentulous patients
- Angle's Class I skeletal relationship
- Normal facial symmetry
- Cooperative patients
You will not qualify if you...
- Temporomandibular disorders
- Uncontrolled diabetes
- Patients with neuromuscular disorders
- Severe psychiatric disorders
- Angle's class II and III skeletal relationship
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Faculty of dentistry-Cairo university
Cairo, Egypt, 22022
Actively Recruiting
Research Team
L
Lujayn A Mahmoud, BDS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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