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CompletedNCT07643441Updated Sep 16, 2026

Accuracy of Complete-Arch Implant Photogrammetry

An observational study in Edentulous Jaw, sponsored by Menoufia University. Completed at 1 site in Egypt. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-09-16.

Sponsored by Menoufia University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
24
Ages
18 Years to 50 Years
Sex
All
01

Study summary

This prospective comparative clinical study evaluated the accuracy and chairside time of complete-arch implant scans obtained using an intraoral photogrammetry system and a mobile-phone-based photogrammetry system in edentulous patients rehabilitated with complete-arch implant-supported prostheses. Implant positions recorded by each system were compared with a reference dataset to assess linear and angular discrepancies. The chairside time required for data acquisition was also measured. The study aimed to determine whether mobile-phone-based photogrammetry can provide clinically acceptable accuracy comparable to that of intraoral photogrammetry while improving clinical efficiency. The findings may help clinicians select appropriate digital impression techniques for complete-arch implant rehabilitation.

Read the detailed description

Accurate recording of implant positions is essential for the passive fit and long-term success of complete-arch implant-supported prostheses. Photogrammetry-based technologies have emerged as promising alternatives to conventional digital impression techniques for capturing implant positions with high accuracy. While intraoral photogrammetry systems have demonstrated favorable results, the clinical performance of recently introduced mobile-phone-based photogrammetry systems remains insufficiently investigated.

This prospective comparative clinical study aims to evaluate the accuracy and chairside time of complete-arch implant scans obtained using an intraoral photogrammetry system and a mobile-phone-based photogrammetry system in edentulous patients restored with complete-arch implant-supported prostheses. Each participant will undergo implant scanning using both systems according to the manufacturers' recommendations. The resulting digital datasets will be compared with a reference dataset to determine scan accuracy.

The primary outcome measures will be linear and angular discrepancies between the implant positions captured by each photogrammetry system and the reference dataset. Secondary outcome measures will include the chairside time required for scan acquisition. Statistical analyses will be performed to compare the accuracy and efficiency of the evaluated systems.

02

Conditions studied

  • Edentulous Jaw

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03

In context

Jaw, Edentulous

171 studies on the registry are indexed under Jaw, Edentulous; 24 are open to participants now.

This study's enrollment of 24 is below the median of 40 across 25 observational studies indexed under Jaw, Edentulous.

Browse Jaw, Edentulous studies →

Lead sponsor

Menoufia University is the lead sponsor of 192 studies on the registry; 53 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

The study population will consist of adult completely edentulous patients who have been rehabilitated with implant-supported complete-arch prostheses. Eligible participants will present with a fully edentulous arch restored by at least four osseointegrated dental implants and will be recruited from patients seeking prosthodontic treatment and follow-up care at the study center. All participants will undergo complete-arch implant scanning using both an intraoral photogrammetry system and a mobile-phone-based photogrammetry system for comparative evaluation of scan accuracy and chairside acquisition time. Only patients meeting the predefined inclusion criteria and providing written informed consent will be enrolled.

Inclusion criteria

  • Adults aged 18 years or older.
  • Completely edentulous patients rehabilitated with implant-supported complete-arch prostheses.
  • Presence of at least four osseointegrated implants in the edentulous arch.
  • Patients able to undergo digital implant scanning procedures.
  • Patients willing to participate and provide written informed consent.

Exclusion criteria

Exclusion Criteria:

  • Patients with unstable or failed implants.
  • Presence of peri-implant disease, active oral infection, or significant soft-tissue inflammation around the implants.
  • Inadequate access for placement of photogrammetry scan bodies or markers.
  • Patients with conditions that prevent proper scanning procedures (e.g., inability to maintain mouth opening or remain still during data acquisition).
  • Patients requiring immediate implant placement or immediate loading protocols.
  • Patients unwilling or unable to provide informed consent.
  • Incomplete clinical records or inability to complete all study procedures.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
24 participants (actual)
Patient registry
No

Groups and cohorts

  • Intraoral Photogrammetry (IPG)

    Participants will undergo complete-arch implant scanning using an intraoral photogrammetry system (IPF Elite, Shining 3D). Implant positions will be digitally recorded according to the manufacturer's instructions. Linear and angular discrepancies relative to the reference dataset, as well as chairside scanning time, will be evaluated.

    Device: Intraoral Photogrammetry (IPG)

  • Mobile-Phone-Based Photogrammetry

    Participants will undergo complete-arch implant scanning using a mobile-phone-based photogrammetry system (T-Marker). Implant positions will be digitally recorded according to the manufacturer's instructions. Linear and angular discrepancies relative to the reference dataset, as well as chairside scanning time, will be evaluated.

    Device: Mobile-Phone-Based Photogrammetry

Interventions

  • DeviceIntraoral Photogrammetry (IPG)

    A photogrammetry-based digital impression system used to capture the three-dimensional positions of implants in complete-arch rehabilitations. The system records implant locations through specialized scan bodies and generates a digital dataset for subsequent accuracy analysis.

    Also known as: IPF Elite; Shining 3D; Intraoral Photogrammetry System

  • DeviceMobile-Phone-Based Photogrammetry

    A smartphone-assisted photogrammetry system used to capture the three-dimensional positions of implants in complete-arch rehabilitations. The system acquires photographic data through coded markers and generates a digital dataset for subsequent accuracy analysis.

    Also known as: T-Marker; Extraoral Photogrammetry; Mobile-Phone-Based Photogrammetry System

06

What researchers measure

Primary outcomes

  1. Linear Discrepancy of Complete-Arch Implant Scans

    Assessment of the linear deviation (μm) between implant positions captured using intraoral photogrammetry and mobile-phone-based photogrammetry systems and those recorded in the reference dataset. Lower values indicate greater accuracy.

    Time frame: Immediately after scan acquisition and digital analysis (same study visit).

07

Study locations

1 site
  • Mohammed El-Sawy
    Shibīn al Kawm, Menoufia 2266166, Egypt
08

References and documents

Individual participant data

Plan to share: No — Up on resonable request from the corresponding author

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07643441
Lead sponsor
Menoufia University
Collaborators
Mansoura University
Responsible party
Mohammed El-Sawy (Dr, Menoufia University) — Principal investigator
First posted
Jun 11, 2026
Start date
Jan 1, 2026
Primary completion
Jun 1, 2026
Completion
Aug 1, 2026
Last update
Sep 16, 2026

Study contacts

Mohammed A. El-Sawy, PhD
principal investigator · Menoufia University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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