Accuracy of Complete-arch Implant Scans Obtained Using T-Marker
1 other identifier
interventional
24
1 country
1
Brief Summary
This randomized crossover clinical study will evaluate and compare the accuracy and effective scanning time of complete-arch implant scans obtained using the (TruAbutment,Marker) T-Marker photogrammetry application operated on a smartphone and a tablet. Twenty-four patients with completely edentulous arches rehabilitated with four well-integrated implants connected to multiunit abutments will undergo both digital impression protocols in a randomized sequence. A verified conventional implant cast will serve as the reference standard. Linear and angular deviations between the implant positions obtained using each digital protocol and the reference model will be evaluated using three-dimensional analysis software. Effective scanning time required for implant coordinate acquisition and registration will also be recorded. The study will determine whether the use of T-Marker with a smartphone provides accuracy and scanning efficiency comparable to its use with a tablet.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Aug 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2026
CompletedFirst Submitted
Initial submission to the registry
September 8, 2026
CompletedFirst Posted
Study publicly available on registry
September 16, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 1, 2027
September 16, 2026
September 1, 2026
6 months
September 8, 2026
September 11, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Angular deviation of complete-arch implant scans
Angular deviation of the implant positions obtained using T-Marker photogrammetry with a smartphone or tablet, compared with the reference implant positions obtained from the verified conventional splinted impression. Angular deviation will be measured in degrees using three-dimensional inspection software.
Immediately after each digital impression procedure
Secondary Outcomes (1)
Linear deviation of complete-arch implant scans
Immediately after each digital impression procedure
Study Arms (2)
T-Marker With Smartphone
EXPERIMENTALParticipants undergo complete-arch implant scanning using T-Marker optical markers attached to the multiunit abutments and a smartphone-based photogrammetry workflow.
T-Marker With Tablet
EXPERIMENTALParticipants undergo complete-arch implant scanning using T-Marker optical markers attached to the multiunit abutments and a Tablet-based photogrammetry workflow.
Interventions
Complete-arch implant positions are captured using T-Marker optical markers attached to the multiunit abutments and a smartphone-based photogrammetry workflow. An iPhone 15 Pro Max running the T-Marker application is used to acquire and register the implant positions.
Complete-arch implant positions are captured using T-Marker optical markers attached to the multiunit abutments and a tablet running the T-Marker application. The system captures and registers the three-dimensional positions of the four implants.
Eligibility Criteria
You may qualify if:
- Adults aged 40-60
- Completely edentulous maxillary arch.
- Four well-integrated dental implants connected to multiunit abutments.
- Implants positioned in the right and left canine and molar regions.
- Presence of a screw-retained interim implant-supported prosthesis or need for definitive implant-supported prosthetic rehabilitation.
- Willingness to provide written informed consent.
You may not qualify if:
- Fewer than four implants.
- Implants placed in the mandibular arch.
- Failed implants.
- Active peri-implant infection or suppuration
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Mohammed Elsawy
Shibīn al Kawm, Menoufia, 2266166, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- No participants, care providers, investigators, or outcome assessors will be masked to the digital impression device used.
- Purpose
- OTHER
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Lecturer of Prosthodontics
Study Record Dates
First Submitted
September 8, 2026
First Posted
September 16, 2026
Study Start
August 1, 2026
Primary Completion (Estimated)
February 1, 2027
Study Completion (Estimated)
March 1, 2027
Last Updated
September 16, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share
Up on reasonable request from the corresponding author.