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Evaluation of the Accuracy of Full Digital Workflow for Guided Implant Surgery Using the R2 Gate Software

Not Applicable
Completed
Conditions
Partially Edentulous Maxilla
Partially Edentulous Mandible
Interventions
Procedure: Full digital workflow
Procedure: Partially digital workflow
Registration Number
NCT03814655
Lead Sponsor
Concordia Dent Srl
Brief Summary

The primary aim of the present study is to compare the accuracy of a full digital workflow for dental implants insertion to a partially digital workflow, for a limited edentulous space (1 to 3 dental units), in the maxilla or mandible.

Detailed Description

Improvements of dental digital technologies are nowadays enabling clinicians to take the digital impressions of the dental arches, therefore avoiding the use of conventional impression materials. Digital impression procedures are claimed to be an approach to improve the accuracy of dental restorations by minimizing the error prone to conventional impression and gypsum model casting, enabling a high degree of standardization. Patients often prefer intraoral scan when compared to the traditional impression. Digital impression is also recommended when patients have remaining teeth that are extremely mobile or misaligned, due to the risk of exfoliation during the conventional impression procedure.

Despite its poor scientific and clinical evidence, the use of digital technologies into the daily practice registers a rapidly growing.

The precision of digital impressions depends on two different parameters: the resolution of the optical scanning system, and the precision of the matching algorithm which may significantly influence the precision of full arch scans. In order to minimize the effect of matching artifacts, only small parts of the dental arch in close vicinity of the teeth are recommended to be scanned.

For prosthetic restoration purpose, several studies regarding the accuracy of digital vs analogue impression have been performed, but none comparing the accuracy of digital vs partially digital workflow for prosthetically driven guided dental implant insertion.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
54
Inclusion Criteria
  • Kennedy Class III partially edentulism with 3 or less missing teeth,
  • Good general health with no contraindications for implant surgery,
  • Acceptance of dental implant treatment,
  • Acceptance of 1 or 2 CBCTs.
Exclusion Criteria
  • Limited bone volume with stadial bone graft requirement,
  • Limited mouth opening (impossible to use the surgical stent),
  • Parkinson disease (impossible to perform an accurate CBCT).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Full digital workflowFull digital workflow1. Intraoral scan of the partially edentulous site, antagonists and occlusion registration. Radiopaque tray customization over the partially edentulous arch. 2. CBCT with customized radiopaque tray. 3. Merging files in R2 Gate software and implant planning. 4. Guided implant insertion with immediate loading, if possible. Megagen dental implants will be inserted. 5. Digital impression for final screw-retained crown/bridge. 6. Assessment of accuracy by comparing stl files (planned and postimplant insertion).
Partially digital workflowPartially digital workflow1. Impression of the edentulous arch and antagonist, occlusion registration. Radiopaque tray customization over the edentulous arch. 2. CBCT with customized radiopaque tray. 3. Stone models alone, maximum intercuspal position and customized radiopaque tray will be scanned using a desktop scanner. 4. Merging files (CBCT and model stl) in R2 Gate software and implant planning. 5. Guided implant insertion with immediate loading, if possible. Megagen dental implants will be inserted. 6. Classic impression in customized tray with Impregum. 7. Functional models will be scanned using the same desktop scanner. 8. Final screw-retained crown/bridge manufacturing. 9. Assessment of accuracy by comparing stl files (planned and postimplant insertion).
Primary Outcome Measures
NameTimeMethod
Accuracy of dental implant insertion6 weeks

Accuracy is described, by the International Organization for Standardization (ISO) standard 5725-1, through the use of two parameters: trueness and precision.

Trueness refers to the deviation between the actual dimension of the measured object and the resulting measurement, while precision indicates how closely repeated the measurements in a set are.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

"Carol Davila"University of Medicine and Pharmacy

🇷🇴

Bucharest, Romania

Concordia Dent Clinic

🇷🇴

Bucharest, Romania

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