Precision of Complete-arch Digital Implant Impressions With Intraoral Scanning Versus Photogrammetry

William Negreiros

Status: Completed

Conditions: Edentulous Jaw

Treatments: Other: Photogrammetry; Other: Digital scanning

Study type: Interventional

Funder types: Other

Identifiers

NCT05972148

IRB18-0660

Details and patient eligibility

About

The goal of this cross-over clinical trial is to investigate the precision of digital implant impressions using an intraoral scanner and photogrammetry in obtaining complete-arch implant-supported scans.

The main question[s] it aims to answer are:

• Is there a difference in precision between intraoral scans and photogrammetry in obtaining digital implant scans?
• Will arch perimeter and jaw type (maxilla vs. mandible) affect the precision results?

Procedures: At each appointment, participants existing permanent/temporary prosthesis or healing caps were unscrewed and temporarily removed for the period of the consultation appointment.

Scanbodies were screwed into their implants for the duration of the appointment.

They underwent two types of digital implant impression procedures (five times each), including intraoral scan and photogrammetry.

Intraoral and extraoral photography were taken.

At the end of each appointment, the scanbodies were removed, and existing bridge/healing caps were reinserted.

The procedures were not painful or required any form of local anesthetic

Comparison group: Researchers compared the precision of intraoral scanning vs. photogrammetry to see which device provided the best precision outcomes.

Enrollment: 22 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Present with a completely edentulous arch with at least four implants
• Have bone-level implants
• Intended for restoration with a screw-retained abutment-level fixed implant-supported prosthesis.

Exclusion criteria

• Patients unable to tolerate the digital scans impressions
• Presented with implants other than bone-level platforms
• Not intended for restorations with screw-retained abutment-level fixed implant-supported prosthesis
• Not completely edentulous.

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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22 participants in 2 patient groups

Intraoral Scanning

Active Comparator group

Treatment:

Other: Digital scanning

Photogrammetry Scanning

Experimental group

Treatment:

Other: Photogrammetry