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NCT04213443 Clinical Trial

Fetal Growth Pattern in Short Stature Women

Intrauterine Growth Restriction Clinical Trial

Official title:
Fetal Growth Pattern in Short Stature Women as a Model for True Intrauterine Growth Restriction Prediction.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04213443
Other study ID # 0275-19-RMB
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 31, 2020
Est. completion date March 11, 2021

Study information
Verified date March 2021
Source Rambam Health Care Campus
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Women of short stature tend to be classified regarding fetal growth by the same criteria as women of normal and tall stature. The objective of the following study is to evaluate fetal growth patterns parallel to women's height and try to make conclusions regarding possible definitions of subjective Intra-uterine growth restriction.

Description:

Based on a patient registry, women of short stature tend to be classified regarding fetal growth by the same criteria as women of normal and tall stature. The objective of the following study is to evaluate fetal growth patterns parallel to women's height and try to make conclusions regarding possible definitions of subjective Intra-uterine growth restriction. Informed consent is not required due to the retrospective nature of the study. Patient information including medical, obstetric and general background will be collected.

Recruitment information / eligibility
Status Completed
Enrollment 200
Est. completion date March 11, 2021
Est. primary completion date February 28, 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Women under 1.6 meters of height. - Singleton pregnancy. - Low risk pregnancy. - Accurate dating. Exclusion Criteria: - Women over 1.6 meters of height. - Multiple pregnancy. - High risk pregnancy.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Analysis of a patient registry
Analysis of a patient registry.

Locations
Country Name City State
Israel Rambam health care campus Haifa

Sponsors (1)
Lead Sponsor Collaborator
Rambam Health Care Campus

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Estimated fetal weight changes. Changes in estimated fetal weight during pregnancy. Up to 1 year from admission.
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