Dental and Oral Finding in Israeli Children With Past Intrauterine Growth Retardation (IUGR)

March 23, 2009 updated by: Hadassah Medical Organization

Dental and Oral Findings in Israeli Children With Past IUGR - a Comprehensive Study

oral status and early childhood caries (ecc) in israeli children with past IUGR

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Anticipated)

45

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

  • Israel
      • Jerusalem, Israel, 91120
        • Hadassah Medical Organization
        • Contact:
        • Principal Investigator:
          • Joseph Shapira, DMD
        • Principal Investigator:
          • Evelyn Mamber, DMD
        • Sub-Investigator:
          • Chen Sela, PhD
        • Sub-Investigator:
          • Hadas Katz-Sagi, DMD
        • Sub-Investigator:
          • Rinat Zach

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

3 years to 4 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

15 children aged 3-4 y old with IUGR in the past, 30 healthy children sex and age matched

Description

Inclusion Criteria:

  • children who were born and diagnosed with IUGR

Exclusion Criteria:

  • children whos mothers have been diagnosed with diabetes or high blood pressure children with genetic disorders multiple babies pregnancy

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
past IUGR
3-4 y old children with past IUGR
Other: no intervention
no intervention
Other Names:
  • ECC
  • past IUGR
control
3-4 y old healthy children
Other: no intervention
no intervention
Other Names:
  • ECC
  • past IUGR

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
oral status of children with past IUGR
Time Frame: 1 year
1 year

Collaborators and Investigators

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

Sponsor

Hadassah Medical Organization

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

June 1, 2009

Primary Completion (Anticipated)

December 1, 2009

Study Completion (Anticipated)

February 1, 2010

Study Registration Dates

First Submitted

March 22, 2009

First Submitted That Met QC Criteria

March 23, 2009

First Posted (Estimate)

March 24, 2009

Study Record Updates

Last Update Posted (Estimate)

March 24, 2009

Last Update Submitted That Met QC Criteria

March 23, 2009

Last Verified

March 1, 2009

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • iugr2009HMO-CTIL

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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