Clinical Trial

Scan Time and Prosthetic Complications of Intraoral Scanning Versus Intraoral Photogrammetry for Full-Arch Titanium Framework With Zirconia Overlay Implant Screw-Retained Prostheses

Recruiting
View on ClinicalTrials.gov →
Record status
This record was last updated March 3, 2026 (before its estimated June 2026 completion). Its status may not reflect the trial's current state.
Summary
This study aims to evaluate the effect of intra-oral scanning and intra-oral photogrammetry on scan time and prosthetic complications in patients receiving full-arch titanium framework with zirconium overlay implant screw-retained prostheses. Participants will: Receive a full arch implant prosthesis and scan time will be recorded. Prosthetic complications (e.g., screw loosening, framework fracture, zirconia chipping) will be recorded at 3 and 6-month follow-up period post-delivery and we will manage complications at the time of prosthetic complication occurrence.
Trial Details
NCT Number NCT07446790
Lead Sponsor Cairo University
Conditions Scan Time
Enrollment 11 participants
Start Date 2025-08-01
Primary Completion 2026-06 (estimated)
Study Completion 2026-06 (estimated)
Updated on ClinicalTrials.gov 2026-03-03