Molar Incisor Malformation in Egypt

April 28, 2023 updated by: Maha Moussa Azab, Fayoum University

Prevelance of Molar Incisor Malformation in Egypt

The aim of the current study is to assess the prevalence of molar incisor malformation in Fayoum-Egypt.

Study Overview

Status

Completed

Detailed Description

Localized developmental radicular dysplasia is a rare finding. This radicular formation arrest may be due to traumas, infections, radiation therapy, chemotherapy, or idiopathic.

Molar Incisor Malformation is a condition characterized by arrested or altered radicular development of first permanent molars. Roots may be thin, short, or totally missing. In some patients, there are constrictions located in the cervical part of the crown of the permanent incisors. There are also cases where the roots of the second primary molars are affected.

MIM could also have been mistaken for a consequence of severe root resorption, or dentine dysplasia prior to its initial description.

This unique deformity, regardless of its nomenclature, presents previously undescribed clinical features and it is quite difficult to get a successful conservative treatment result.

The aim of the current study is to assess the prevalence of this rare condition in Fayoum-Egypt.

Study Type

Observational

Enrollment (Actual)

5630

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

      • Fayoum, Egypt
        • Alpha Dent

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

No

Sampling Method

Non-Probability Sample

Study Population

panoramic radiographic images from a private dental radiology center in Fayoum Egypt

Description

Inclusion Criteria:

  • Panoramic radiographs for older than nine-year-old patients, having completely developed first permanent molars

Exclusion Criteria:

  • Panoramic radiographs with missing first permanent molars or pathological lesions which may cause root resorption

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
1
older than 9-year-old patients, with panoramic radiographic images showing the first permanent molars
the presence of radiographic features of molar incisor malformation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
molar incisor malformation
Time Frame: Day 1
the presence of root malformation to indicate the diagnosis of molar incisor malformation
Day 1

Collaborators and Investigators

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

Investigators

  • Principal Investigator: maha M azab, Fayoum 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)

May 30, 2022

Primary Completion (Actual)

March 1, 2023

Study Completion (Actual)

March 1, 2023

Study Registration Dates

First Submitted

April 28, 2023

First Submitted That Met QC Criteria

April 28, 2023

First Posted (Actual)

May 8, 2023

Study Record Updates

Last Update Posted (Actual)

May 8, 2023

Last Update Submitted That Met QC Criteria

April 28, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Molar Incisor Malformation

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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