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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00333333
Other study ID # CCC# 26075
Secondary ID
Status Completed
Phase N/A
First received June 2, 2006
Last updated June 12, 2008
Start date June 2006
Est. completion date June 2008

Study information

Verified date June 2008
Source Christiana Care Health Services
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This research project is studying the causes for low platelet levels in preterm infants. Platelets are a component of blood that helps with clotting. The purpose of this study is to determine whether the cause for low platelet levels is the same in infants who are born to mothers with preeclampsia and infants who are small for gestational age.


Description:

Thrombocytopenia is a common entity in infants who are born to mothers with preeclampsia and in infants who are small for gestational age. There have been several theories to the mechanism underlying thrombocytopenia in these groups of patients. One mechanism suggests that thrombocytopenia in these populations may be secondary to underproduction of platelets. Other studies have implied that low platelet levels may be due to endothelial activation causing platelet consumption. This study is being performed to help determine the mechanism causing thrombocytopenia in infants born to mothers with preeclampsia and comparing it to the mechanism of thrombocytopenia in infants who are small for gestational age.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 2008
Est. primary completion date March 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Infants who are less than 34 weeks gestation

- Infants born to mothers with preeclampsia

- Infants who are born small for gestational age whose mother did not have preeclampsia

Exclusion Criteria:

- Infants who are greater than 34 weeks gestation

- Infants with known congenital anomalies or known congenital infections

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Intervention

Procedure:
Cord blood
Cord blood will be obtained at the time of delivery.

Locations

Country Name City State
United States Christiana Care Health Systems Newark Delaware

Sponsors (2)

Lead Sponsor Collaborator
Christiana Care Health Services The Cardeza Foundation for Hematologic Research

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To determine the mechanism of thrombocytopenia in small for gestational age infants versus infants with maternal preeclampsia exposure Each infant will only be enrolled during the time of birth until cord blood is collected. No
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