Intraoral Scanner With and Without Orthodontic Brackets

August 19, 2024 updated by: Abdulrahman Majed Ahmed Joureyah, Cairo University

Effect of Two Different Intraoral Scanners on the Scanning Quality and Time in Patients With/Without Orthodontic Brackets

this study aim to evaluate the effect of two different intraoral scanners on the scanning Quality and Time in Patients With/Without Orthodontic Brackets

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

aim of study : evaluate two types of Intra-oral scanner in patients with/without orthodontics brackets

methodology:

  • patient preparation diagnosis, photos, x-rays
  • starting scanning in 3 techniques bucco-palatal , palato-buccal ,s shape
  • brackets bonding by indirect technique
  • scanning after brackets placement also by same 3 techniques
  • data measurements by linear and angular measurements.

outcome:2 scanners will be evaluated

Study Type

Observational

Enrollment (Actual)

10

Contacts and Locations

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

Study Locations

  • Egypt
      • Cairo, Egypt
        • Faculty of Dentistry, Cairo University

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

Accepts Healthy Volunteers

N/A

Sampling Method

Probability Sample

Study Population

full permenant dentition with mild to moderate crowding

Description

Inclusion Criteria:

  1. Patients of both sexes.
  2. Full permanent dentition cases.
  3. Class I/II/III molar relationship.
  4. Mild to moderate crowding cases

Exclusion Criteria:

  1. Dental anomalies.
  2. Congenital missing teeth.
  3. Impaction.
  4. Orthognathic surgery

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
compare the readings resulted from the models produced from the 3 scanners (2 intraoral scanners + the desktop scanner) before bonding and to compare the 2 intraoral scanners after bonding.
Time Frame: 3 to 4 weeks
using 3 techniques Bucco-palatal, Palato-buccal, S-shape technique collect data and using linear , teeth dimension measurements and angular measurements in 3 shape orthodontic software for data analysis linear measurements will be maxillary/ mandibular inter canine width, maxillary/mandibular inter premolar width , maxillary/mandibular inter molar width , maxillary/ mandibular anterior arch length , maxillary/ mandibular total arch length secondly teeth dimensions by 3shape orthodontic software by measure each tooth from mesial to distal
3 to 4 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
compare the readings resulted from the models produced from the 2 scanners with and without orthodontic brackets.
Time Frame: 3 to 4 weeks
measure according to repeatedly scans done by 2 different intra-oral scanners (primescan and carestream) on dental arch using 3 techniques bucco-palatal, palato-buccal and s shape before bonding brackets and after bonding then used 3 shape orthodontic software to superimpose the repeatedly scans on the dental arch either primescan or carestream using ( accuracy and precision) to see if the scans appears clear or deviated with / without brackets
3 to 4 weeks

Collaborators and Investigators

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

Sponsor

Cairo University

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)

June 15, 2022

Primary Completion (Actual)

June 24, 2023

Study Completion (Actual)

September 3, 2023

Study Registration Dates

First Submitted

March 15, 2024

First Submitted That Met QC Criteria

March 29, 2024

First Posted (Actual)

April 2, 2024

Study Record Updates

Last Update Posted (Actual)

August 21, 2024

Last Update Submitted That Met QC Criteria

August 19, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 30723

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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