Actively Recruiting

Phase Not Applicable
All Genders
NCT06846619

"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

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Completely edentulous patients
  • Angle's Class I skeletal relationship
  • Normal facial symmetry
  • Cooperative patients
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Faculty of dentistry-Cairo university

Cairo, Egypt, 22022

Actively Recruiting

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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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