Actively Recruiting
Patient Satisfaction of Intra-orally Scanned Versus Extra-orally Scanned Digitally Printed Maxillary Denture in Completely Edentulous Patients, in Vivo Study.
Led by Cairo University · Updated on 2025-02-26
8
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating patient satisfaction with two types of digitally printed maxillary dentures in patients who have no natural teeth (completely edentulous). This study compares dentures made from intra-oral digital scans taken directly inside the mouth versus those made from extra-oral digital scans created from traditional impressions taken outside the mouth. The goal is to understand if one scanning method leads to better comfort, fit, aesthetics, and overall satisfaction for patients. Participants will receive both types of dentures fabricated using 3D printing technology. The intra-oral scanning uses a 3Shape scanner to capture digital impressions directly from the mouth, while the extra-oral scanning involves taking traditional impressions that are then scanned externally. Each participant will wear one type of denture for a period, followed by a two-week wash-out period without dentures, before switching to the other type. After wearing each denture, participants will complete satisfaction surveys. During the study, participants will be assessed for comfort, fit, and aesthetics of each denture type using structured questionnaires. Satisfaction will be measured after six months of wearing each denture, with the two-week wash-out period separating interventions. Data from these assessments will be analyzed to identify any significant differences in patient preferences. The study duration includes these treatment and evaluation phases and aims to provide evidence to guide clinical choices for denture fabrication.
CONDITIONS
Brief 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
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 6 months for each denture
Participants will receive maxillary dentures fabricated using either intra-oral or extra-oral scanning methods. They will wear one type of denture for a specified period and provide feedback through structured satisfaction surveys.
2 denture delivery visits and satisfaction assessments after each denture use
Duration - 2 weeks
Participants will not wear dentures for a two-week wash-out period between using the two types of dentures to ensure no overlap effects.
No visits during this period
Trial Site Locations
Total: 1 location
1
Faculty of dentistry-Cairo university
Cairo, Egypt, 22022
Actively Recruiting
Research Team
L
Lujayn A Mahmoud, BDS
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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