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

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2009 by Hadassah Medical Organization.
Recruitment status was  Not yet recruiting
Sponsor:
Information provided by:
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT00867542
First received: March 22, 2009
Last updated: March 23, 2009
Last verified: March 2009
  Purpose

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


Condition Intervention
Dental Caries
Other: no intervention

Study Type: Observational
Study Design: Time Perspective: Retrospective
Official Title: Dental and Oral Findings in Israeli Children With Past IUGR - a Comprehensive Study

Resource links provided by NLM:


Further study details as provided by Hadassah Medical Organization:

Primary Outcome Measures:
  • oral status of children with past IUGR [ Time Frame: 1 year ] [ Designated as safety issue: No ]

Estimated Enrollment: 45
Study Start Date: June 2009
Estimated Study Completion Date: February 2010
Estimated Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
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

  Eligibility

Ages Eligible for Study:   3 Years to 4 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
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

Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00867542

Contacts
Contact: Hadas Katz-Sagi, DMD 97226776168 hadaskatzsagi@gmail.com
Contact: Hadas Lemberg, PhD 00 972 2 6777572 lhadas@hadassah.org.il

Locations
Israel
Hadassah Medical Organization Not yet recruiting
Jerusalem, Israel, 91120
Contact: Arik Tzukert, DMD    : 00 972 2 6776095    arik@hadassah.org.il   
Contact: Hadas Lemberg, PhD    00 972 2 6777572    lhadas@hadassah.org.il   
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         
Sponsors and Collaborators
Hadassah Medical Organization
  More Information

No publications provided

Responsible Party: Hadassah Medical Organization, Jerusalem, Israel
ClinicalTrials.gov Identifier: NCT00867542     History of Changes
Other Study ID Numbers: iugr2009HMO-CTIL
Study First Received: March 22, 2009
Last Updated: March 23, 2009
Health Authority: Israel: Ministry of Health

Keywords provided by Hadassah Medical Organization:
past IUGR
ECC
oral findings in children with past IUGR

Additional relevant MeSH terms:
Dental Caries
Fetal Growth Retardation
Fetal Diseases
Growth Disorders
Pathologic Processes
Pregnancy Complications
Stomatognathic Diseases
Tooth Demineralization
Tooth Diseases

ClinicalTrials.gov processed this record on November 20, 2014