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UnknownNCT00471575

Fatty Liver in Pregnancy

Prospective Observational Study

Status
Unknown
Phase
Study type
Observational
Enrollment
Sponsor
Assaf-Harofeh Medical Center · Other Government
Sex
Female
Age
18 Years
Healthy volunteers

Summary

Non alcoholic fatty liver disease (NAFLD) is one of the main causes of development of chronic liver disease and cirrhosis. There are no published studies which have investigated the incidence of NAFLD in pregnant women or the correlation between the metabolic changes in pregnancy and this phenomenon. We aimed in our study to explore the incidence of NAFLD in pregnancy by ultrasonography (US) during the end of the pregnancy or immediately after birth (after 36 weeks) and to look for a correlation between fatty liver and demographic, clinical, nutritional and laboratory data during pregnancy.

Detailed description

Fatty liver in pregnancy-protocol: Non alcoholic fatty liver disease (NAFLD) is one of the main causes of development of chronic liver disease and cirrhosis. The incidence of NAFLD among the general population is about 17-30%. There are no published studies which have investigated the incidence of NAFLD in pregnant women or the correlation between the metabolic changes in pregnancy and this phenomenon. We aimed in our study to explore the incidence of NAFLD in pregnancy by ultrasonography (US) during the end of the pregnancy or immediately after birth (after 36 weeks) and to look for a correlation between fatty liver and demographic, clinical, nutritional and laboratory data during pregnancy. Methods: US examination will be performed by an experienced technician. The liver will be scanned by B mode US using a 2-5 MHZ transducer. In those with fatty liver as seen by US, a repeat examination will be performed after 6 weeks and 24 weeks. For women with the diagnosis of fatty liver, serum lipid profile, glucose, liver function tests and insulin will be done. Homa score as well as BMI will be calculated for each woman with fatty liver. All participants will sign an informed consent which has been approved by the hospital ethical committee.

Conditions

Interventions

TypeNameDescription
PROCEDUREultra sound examination

Timeline

Start date
2007-06-01
Completion
2007-12-01
First posted
2007-05-10
Last updated
2007-05-15

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00471575. Inclusion in this directory is not an endorsement.