Assessment of Decision Support System Software in Extraction and Anchorage Planning Among Adult Patients Using Computer Algorithm

July 18, 2022 updated by: Walaa Mohamed Hassan Gadallah, Cairo University
It was introduced in dentistry to be used in innovative research and development in addition to facilitating the decision in complicated cases and ensure high patient care quality. In the field of Orthodontics in specific, many studies previously mentioned the idea of artificial intelligence showing very promising results and high degree of reliability. It was used in different domains in orthodontics like diagnosis, treatment planning, evaluation of treatment outcome

Study Overview

Detailed Description

In this study, the aim is to access the efficiency of the new decision support system in determining whether the decision is extraction or non-extraction and the anchorage plan required for each case. This was performed in the past in many countries and those studies are published

Study Type

Observational

Enrollment (Anticipated)

80

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

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

15 years to 35 years (Child, Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Recruiting well finished cases having history of crowding from Kasr el Ainy with no severe skeletal discrepancy, cases should be well documented. The precise and complete documentation of the patients in terms of the presence of:

  1. Preoperative and postoperative x-rays.
  2. Good quality preoperative and postoperative photographs.
  3. Preoperative and postoperative study models.
  4. Detailed documentation of the treatment sequence and mechanics. If there were incomplete data provided in the patient's file; the patient will then be excluded from the study.

Description

Inclusion Criteria:

  1. Cases with well finished orthodontic treatment.
  2. Cases with history of crowding more than 10 mm and requiring extraction.
  3. Cases with no severe skeletal discrepancy.
  4. Well documented cases with both pre-operative and post-operative records.
  5. Patients with a full set of permanent teeth erupted

Exclusion Criteria:

  1. Improperly finished orthodontic cases.
  2. Cases with mild crowding managed by treatment options other than extraction.
  3. Growing patients or showing any residual growth remaining in cephalometric analysis
  4. Cases with severe skeletal discrepancy.
  5. Poorly documented cases.
  6. Patients not sticking to anchorage plan

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

  • Observational Models: Cohort
  • Time Perspectives: Other

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
well fininshed cases
To decide whether extraction or non-extraction decision will be made for each case
Other Names:
  • extraction and non-extraction in well finished cases

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To study the efficiency of the program decisions in terms of extraction/non-extraction and Anchorage planning decisions
Time Frame: 1 year
The concordance correlation coefficient would be used to measure the agreement between the 2 methods on the basis of the values (%) assigned for each treatment option by the 2 methods (quantitative data).
1 year

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

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 (Anticipated)

August 22, 2022

Primary Completion (Anticipated)

November 1, 2022

Study Completion (Anticipated)

April 1, 2023

Study Registration Dates

First Submitted

December 21, 2021

First Submitted That Met QC Criteria

April 23, 2022

First Posted (Actual)

April 27, 2022

Study Record Updates

Last Update Posted (Actual)

July 20, 2022

Last Update Submitted That Met QC Criteria

July 18, 2022

Last Verified

July 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 94030405

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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