NCT07200440

Brief Summary

To assess and compare the accuracy of digital scans obtained using three different scanning protocols -conventional scan bodies, Intra-oral photogrammetry, and calibrated scan flags- on completely edentulous dental model with full-arch implants.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Dec 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

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

First Submitted

Initial submission to the registry

February 20, 2025

Completed
7 months until next milestone

First Posted

Study publicly available on registry

October 1, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

December 20, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 20, 2026

Completed
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 20, 2026

Completed
Last Updated

October 1, 2025

Status Verified

September 1, 2025

Enrollment Period

2 months

First QC Date

February 20, 2025

Last Update Submit

September 22, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Accuracy of multiunit abutment positions

    positions and angles of the multiunit abutments

    7 days

Study Arms (4)

conventional scan bodies

ACTIVE COMPARATOR

Digital scans using conventional scan bodies scanned with a desktop scanner.

Procedure: Control

scan bodies scanned with an intra-oral scanner

EXPERIMENTAL

Digital scans using conventional scan bodies scanned with an intra-oral scanner.

Procedure: Intervention 1

intra-oral photogrammetry

EXPERIMENTAL

Digital scans using intra-oral photogrammetry scanned with an intra-oral scanner.

Procedure: Intervention 2

calibrated scan flags

EXPERIMENTAL

Digital scans using calibrated scan flags scanned with an intra-oral scanner.

Procedure: Intervention 3

Interventions

Digital scans using conventional scan bodies scanned with an intra-oral scanner.

scan bodies scanned with an intra-oral scanner

Digital scans using intra-oral photogrammetry scanned with an intra-oral scanner.

intra-oral photogrammetry

Digital scans using calibrated scan flags scanned with an intra-oral scanner.

calibrated scan flags
ControlPROCEDURE

Digital scans using conventional scan bodies scanned with a desktop scanner.

conventional scan bodies

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Edentulous dental model simulating completely edentulous patients.
  • Model containing full-arch implant analogs placed in standardized positions.
  • Access to compatible scan bodies for all three scanning protocols.

You may not qualify if:

  • Dental models with defects, such as fractures or irregularities, that may influence scanning accuracy.
  • Implant analogs placed at non-standardized or inconsistent angles.
  • Scan bodies or equipment showing signs of wear or damage that could compromise results.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (2)

  • Ma B, Yue X, Sun Y, Peng L, Geng W. Accuracy of photogrammetry, intraoral scanning, and conventional impression techniques for complete-arch implant rehabilitation: an in vitro comparative study. BMC Oral Health. 2021 Dec 10;21(1):636. doi: 10.1186/s12903-021-02005-0.

    PMID: 34893053BACKGROUND
  • Buzayan M, Baig MR, Yunus N. Evaluation of accuracy of complete-arch multiple-unit abutment-level dental implant impressions using different impression and splinting materials. Int J Oral Maxillofac Implants. 2013 Nov-Dec;28(6):1512-20. doi: 10.11607/jomi.2958.

    PMID: 24278919BACKGROUND

Central Study Contacts

Mohamed Sherif El Saharty

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
DIAGNOSTIC
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 20, 2025

First Posted

October 1, 2025

Study Start

December 20, 2025

Primary Completion

February 20, 2026

Study Completion

March 20, 2026

Last Updated

October 1, 2025

Record last verified: 2025-09