Assesment of the Accuracy of Surgical Guide Designed From CBCT With Different Voxel Sizes

January 2, 2018 updated by: Mohammed Mohammed Ahmed Elhag, Cairo University

Assesment of the Accuracy of Surgical Guide Designed From CBCT With Different Voxel Size in Computer Guided Implantology Randomized Clinical Trial

Accuracy Of CBCT affected by many factors. On of the most factors the affect the image quality is voxel size. Larger voxel size give a higher accuracy of the images but with higher radiation dose.

The study is to assist the accuracy of surgical guides designed from CBCT with different voxel sizes .

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Accuracy Of CBCT affected by many factors. On of the most factors the affect the image quality is voxel size. Larger voxel size give a higher accuracy of the images but with higher radiation dose.

The study is to assist the accuracy of surgical guides designed from CBCT with different voxel sizes (voxel size 0.4mm & 0.2mm)

Study Type

Interventional

Enrollment (Anticipated)

8

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Egypt
      • Cairo, Egypt, 02
        • Recruiting
        • Cairo University
        • Contact:
        • Principal Investigator:
          • Mohammed Elhag

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • partially edentulous patients seeking for dental implant
  • Bucco-lingual width more than 6 mm
  • Medically free patients

Exclusion Criteria:

  • patients with thin ridges that may need augmentation
  • patients with systematic diseases that may affect bone quality
  • completely edentulous patients
  • patients with limited mouth opening

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Surgical guide designed from voxel size 0.2mm
Surgical guide will be designed based on CBCT voxel size 0.2mm
Active Comparator: Surgical guide designed from voxel size 0.4m
Surgical guide will be designed based on CBCT voxel size 0.4 mm
Other: Surgical guide
Surgical Guide for this group will designed from 0.4mm voxel size

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Angular deviation
Time Frame: Immediate post operative
Evaluation of angular deviation of virtual implant and actual implant positions according to voxel size difference (0.2 mm versus 0.4 mm)
Immediate post operative
Linear deviation
Time Frame: Immediate post operative
Evaluation of linear deviation of virtual implant and actual implant positions according to voxel size difference (0.2 mm versus 0.4 mm
Immediate post operative

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Cairo University

Investigators

  • Principal Investigator: Cairo university, Cairo University, faculty of dentistry

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 1, 2017

Primary Completion (Anticipated)

March 15, 2018

Study Completion (Anticipated)

April 1, 2018

Study Registration Dates

First Submitted

December 13, 2017

First Submitted That Met QC Criteria

January 2, 2018

First Posted (Actual)

January 3, 2018

Study Record Updates

Last Update Posted (Actual)

January 3, 2018

Last Update Submitted That Met QC Criteria

January 2, 2018

Last Verified

December 1, 2017

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • ElhagCUImplant

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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