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
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 Locations
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Jerusalem, Israel, 91120
- Hadassah Medical Organization
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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 |
|---|---|
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past IUGR
3-4 y old children with past IUGR
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no intervention
Other Names:
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control
3-4 y old healthy children
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no intervention
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
oral status of children with past IUGR
Time Frame: 1 year
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1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
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.