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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01630603
Other study ID # MMC14-12
Secondary ID
Status Recruiting
Phase N/A
First received June 18, 2012
Last updated February 11, 2013
Start date July 2012

Study information

Verified date June 2012
Source Meir Medical Center
Contact Ita Litmanovich, MD
Phone 09-7471554
Email litmani@clalit.org.il
Is FDA regulated No
Health authority Israel: Institutional Review Board
Study type Observational

Clinical Trial Summary

Objectives:

1. To determine the incidence of vitamin D deficiency among Israeli pregnant women

2. To access whether maternal vitamin D status affects infant bone strength.

Methods:

1. Vitamin D levels -in cord blood and maternal blood

2. The mother will fill a demographic and nutritional questionnaire

The Infants:

3. Growth assessment of the infants: weight length and head circumference

4. Bone strength measurement by Quantitative Ultrasound (Sunlight Omnisense 7000/8000TM)


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- mother-baby pairs,

- birth week 35-42.

- Jewish and Arab women that read and understand Hebrew.

Exclusion Criteria:

- large neonatal congenital defects.

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Neonatal department Meir Medical Center Kfar Saba
Israel Meir Medical Center Kfar-Saba
Israel Meir Medical Center Kfar-Saba

Sponsors (1)

Lead Sponsor Collaborator
Meir Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bone speed of sound and maternal vitamin D levels first tow days of life No
See also
  Status Clinical Trial Phase
Completed NCT03308487 - Vitamin D Supplementation and Pregnancy Outcomes N/A