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Clinical Trials/NCT03730506
NCT03730506
Unknown
Not Applicable

Assessment of the Accuracy of Surgical Guide Designed From Digital Impression, Dental Model Scanning Using CBCT and Desktop Scanner in Computer Guided Implantology: Randomized Clinical Trial

Cairo University0 sites9 target enrollmentNovember 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Computer Guided Implant
Sponsor
Cairo University
Enrollment
9
Primary Endpoint
Evaluation of angular deviation of virtual implants and actual implant position by 3rd party software in degrees
Last Updated
7 years ago

Overview

Brief Summary

Assessment of the Accuracy of Surgical Guide Designed from Digital Impression, Dental Model Scanning using CBCT and Desktop Scanner in Computer Guided Implantology:

Randomized Clinical Trial.

Detailed Description

Research question: In computer guided Implantology, are surgical stents designed from scan of dental model by CBCT and from digital impression as accurate as surgical stents designed from desktop scanner? Statement of the problem: The role digital dentistry is improved in computer guided implantology especially with development of computer guided implant software, desktop scanner and intra oral scanner development and CBCT machines. Intra-oral scanner, desktop scanner and CBCT scanner can be used in creation of 3D digital model that can be used with computer guided implant in fabrication of the surgical stent. And the question, is the accuracy of surgical guide will be affected when designed by one of these different modalities? Rationale for conducting the research: Digital 3D dentoginival details are very important in computer guided implantology and designing of surgical stent.nowadays there are many methods to obtain this soft tissue replica as CBCT,desktop scanner and intra oral scanner.this study is conducted to asses the effect of different method of soft tissue digitization on the accuracy of surgical template used in computer guided implantology.

Registry
clinicaltrials.gov
Start Date
November 2018
End Date
July 2020
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amr taha Adu el wafa

teaching assistant

Cairo University

Eligibility Criteria

Inclusion Criteria

  • partially edentulous patient.
  • Patients with bucco-lingual bone thickness more than 6 mm allowing flapless implant placement.

Exclusion Criteria

  • Completely edentulous patient or Free end saddle edentulous area.
  • Patients needing graft or sinus lifting with implant placement.
  • Patients with thin ridges.
  • Patients with systemic disease that may affect bone quality.
  • Patients with poor oral hygiene and active periodontal diseases.
  • Patient with limited mouth opening

Outcomes

Primary Outcomes

Evaluation of angular deviation of virtual implants and actual implant position by 3rd party software in degrees

Time Frame: one year

Evaluation of angular deviation of virtual implants and actual implant position by 3rd party software in degrees to assess the accuracy of surgical guide

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