NCT06846619 "Patient Satisfaction with Intra-Oral Vs. Extra-Oral Scanned 3D-Printed Dentures: an in Vivo Study"
| NCT ID | NCT06846619 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Cairo University |
| Condition | Complete Edentulism |
| Study Type | INTERVENTIONAL |
| Enrollment | 8 participants |
| Start Date | 2023-12-03 |
| Primary Completion | 2025-09-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 8 participants in total. It began in 2023-12-03 with a primary completion date of 2025-09-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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.
Eligibility Criteria
Inclusion Criteria: * Completely edentulous patients * Angle's Class I skeletal relationship * Normal facial symmetry * Cooperative patients Exclusion Criteria: * -Temporomandibular disorders * Uncontrolled diabetes * Patient's with neuromuscular disorders * Severe psychiatric disorders * Angle's class II and III skeletal relationship.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06846619 clinical trial?
This trial is open to participants of all sexes, studying Complete Edentulism. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06846619 currently recruiting?
Yes, NCT06846619 is actively recruiting participants. Contact the research team at Lujaynamr@dentistry.cu.edu.eg for enrollment information.
Where is the NCT06846619 trial being conducted?
This trial is being conducted at Cairo, Egypt.
Who is sponsoring the NCT06846619 clinical trial?
NCT06846619 is sponsored by Cairo University. The trial plans to enroll 8 participants.