Clinical Trials Directory

Trials / Completed

CompletedNCT00194142

Cytomegalovirus (CMV) Infection in Amniotic Fluid

Status
Completed
Phase
Study type
Observational
Enrollment
37 (actual)
Sponsor
University of Pennsylvania · Academic / Other
Sex
Female
Age
15 Years – 45 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if detection of cytomegalovirus (CMV) in amniotic fluid collected in the second trimester of pregnancy is associated with pregnancy complications such as preterm delivery or severe preeclampsia.

Detailed description

CMV infection in adults with a normal immune system is rarely a serious event. Once a person has been infected with CMV, they may have recurrences (relapses) of the infection. If a mother is infected with the virus or relapses during pregnancy, her fetus may be at risk for infection. Unlike infection in adults, congenital infection may result in serious complications (congenital infection). The effects of fetal infection with CMV are well understood and many efforts have been made to potentially reduce the risk of congenital infection. However, the effect of CMV infection on the pregnancy itself (when the fetus is not affected by CMV) is less understood. The incidence of CMV detection in amniotic fluid collected in the second trimester is thought to be low. However, the association between detection of CMV infection in the second trimester and ultimate pregnancy outcome is poorly described. In this study, we plan to determine if CMV detection in amniotic fluid collected in the second trimester is associated with pregnancy complications.

Conditions

Timeline

Start date
2007-07-01
Primary completion
2008-05-01
Completion
2008-05-01
First posted
2005-09-19
Last updated
2016-08-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00194142. Inclusion in this directory is not an endorsement.