Prevelance of Molar Incisor Hypomineralization Among a Group of Egyptian Children (MIH)

March 1, 2017 updated by: Reem Zaki Youssef, Cairo University

Prevelance of Molar Incisors Hypomineralization Among a Group of Egyptian Children

The purpose of this study is to find out the prevalence of molar incisor hypomineralization among a group of Egyptian children

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Molar incisor hypomineralization is frequent in many population throughout the world and a wide variation of molar incisior hypomineralization 2.4_40% has been reported.To the best of our knowledge,there is no Sufficient information regarding the prevalence of molar incisor hypomineralization in Egyptian children therefore the aim of this study is to assess the prevalence of molar incisor hypomineralization among a group of Egyptian children.

Study Type

Observational

Enrollment (Anticipated)

610

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, 0000
        • Reem Zaki Youssef
      • Cairo, Egypt
        • Reem Zaki Youssef

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

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Group of Egyptian children attending in paediatric dentistry and dental public health department in the faculty of oral and dental medicine,Cairo university

Description

Inclusion Criteria:

- Patient seeks dental care in paediatric dentistry and dental public health department in Cairo university

  • positive patient acceptance for participation in the study
  • children with at least one of four permanent molars erupted or partially erupted

Exclusion Criteria:

  • uncooperative children

    • children with appliance
    • children with systemic diseases

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
Presence of Molar incisor hypomineralization
Time Frame: 10min
Presence of Molar incisor hypomineralization or not through clinical examination (binary)
10min

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Severity of Molar incisor hypomineralization
Time Frame: 15min
Clinical examination using modified index based on EAPD criteria
15min

Collaborators and Investigators

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

Sponsor

Cairo University

Investigators

  • Principal Investigator: Reem Za Youssef, Bechlor, Cairo university

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.

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 (Actual)

February 17, 2017

Primary Completion (Anticipated)

August 1, 2017

Study Completion (Anticipated)

October 1, 2017

Study Registration Dates

First Submitted

February 17, 2017

First Submitted That Met QC Criteria

February 24, 2017

First Posted (Actual)

March 1, 2017

Study Record Updates

Last Update Posted (Actual)

March 3, 2017

Last Update Submitted That Met QC Criteria

March 1, 2017

Last Verified

March 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Ryoussef

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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