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Clinical Trials/NCT07320729
NCT07320729
Active, not recruiting
Not Applicable

Can Intraoral Photogrammetry Overcome Surgical Field Challenges? An In-Vivo Accuracy Study in Immediate Full-Arch Loading

Abdelrahman Khalaf Eldabe1 site in 1 country4 target enrollmentStarted: December 7, 2025Last updated:

Overview

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Abdelrahman Khalaf Eldabe
Enrollment
4
Locations
1
Primary Endpoint
Trueness of Implant Position (3D Euclidean Deviation)

Overview

Brief Summary

This prospective in vivo clinical trial evaluates and compares the accuracy (trueness) and scanning time of intraoral photogrammetry scanners (IPS) versus conventional intraoral optical scanners (IOS) for immediate full-arch implant impressions. The reference standard will be a verified conventional splinted open-tray impression taken at the uncovering stage. Sixty edentulous arches receiving 4-6 implants will be included. Linear, angular, and 3D Euclidean deviations will be calculated to assess accuracy.

Detailed Description

Digital impression systems are widely used for implant dentistry, but complete-arch implant scans remain challenging due to lack of stable landmarks and intraoral movement. Photogrammetry technology captures implant coordinates with high trueness by eliminating stitching errors and excluding unstable soft tissue. A newly introduced intraoral photogrammetry scanner (IPS) integrates photogrammetry and intraoral imaging in a single device.

This study is the first in-vivo prospective clinical trial comparing IOS and IPS accuracy in immediate complete-arch implant loading. Patients receiving 4-6 implants in one arch will undergo two digital impressions immediately after surgery: one using IOS (AoralScan 3) and one using IPS (Elite). A conventional splinted open-tray impression at second-stage surgery will be used as the reference model. Digital files will be superimposed to calculate linear, angular, and 3D (Euclidean) deviations. Scanning time and effect of arch type will also be evaluated.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Completely edentulous arch to receive 4-6 implants. Candidate for immediate loading with a one-piece fixed prosthesis. ASA I or II medically healthy patients. Patient able to attend follow-up visits and sign informed consent.

Exclusion Criteria

  • Medically compromised patients (ASA III or higher). Poor oral hygiene or heavy smokers. Insufficient bone volume for implant placement. Uncooperative patients or those refusing participation.

Outcomes

Primary Outcomes

Trueness of Implant Position (3D Euclidean Deviation)

Time Frame: 3 Months

The primary outcome is to evaluate the clinical performance of conventional intraoral scanners (IOS) and intraoral photogrammetry scanners (IPS) in immediate complete arch implant loading for each patient enrolled in the study, with a paired comparison of the deviation differences (Degree of Trueness).

Secondary Outcomes

  • Effect of Arch Type on Digital Impression Trueness(3 Months)

Investigators

Sponsor
Abdelrahman Khalaf Eldabe
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Abdelrahman Khalaf Eldabe

Lecturer of Oral Medicine and Periodontology , Assiut University

Assiut University

Study Sites (1)

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