Computer-Assisted Removal of Supernumerary Teeth vs Freehand Surgery

February 13, 2026 updated by: Mohamed Farouk Mekky, Kafrelsheikh University

Computer-Assisted Removal of Supernumerary Teeth vs Freehand Surgery : A Randomized Clinical Trial

While CBCT imaging enables the surgeon to precisely map the position of impacted supernumerary teeth relative to neighboring structures, traditional extraction methods for impacted supernumerary teeth can involve extensive bone removal and soft tissue dissection, increasing operative time and trauma. Computer-assisted surgery and the use of 3D-printing technology offer a paradigm shift by leveraging advanced imaging and manufacturing technologies to guide surgical procedures with high accuracy and with and minimally invasive alveolar surgery.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

32

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 Locations

      • Alexandria, Egypt
        • Kafrelsheikh

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • healthy children

Exclusion Criteria:

  • systemic conditions contraindicates 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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: computer guide
extraction of impaction
Placebo Comparator: free hand
extraction of impaction

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
operation time
Time Frame: intraoperative using a stopwatch measuring time in minutes
time from starting of the incision till exposure of the impacted supernumerary
intraoperative using a stopwatch measuring time in minutes

Collaborators and Investigators

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

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)

October 1, 2025

Primary Completion (Actual)

January 28, 2026

Study Completion (Actual)

January 28, 2026

Study Registration Dates

First Submitted

January 29, 2026

First Submitted That Met QC Criteria

February 13, 2026

First Posted (Actual)

February 18, 2026

Study Record Updates

Last Update Posted (Actual)

February 18, 2026

Last Update Submitted That Met QC Criteria

February 13, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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