Prenatal Repository
Condition: Obstetrics
Eligibility
Key Inclusion Criteria
- Pregnant women who have been scheduled for a genetic counseling, chorionic villus sampling (CVS), amniocentesis, ultrasound and/or for clinical reasons
- Offspring of the pregnant women who have participated in this study
- Biological father of the offspring that is the product of current pregnancy
Key Exclusion Criteria
- Women and/or fathers of the fetus who do not wish to participate
- Women and/or fathers of the fetus who are determined by the investigator to be unable to provide informed consent
- Mothers and fathers who are younger than 18 years old
Full Study Name
Perinatal Clinical Data Repository and Tissue Procurement, Storage and Utilization (IRB no. 06806)
Summary
This study focuses on pregnant patients. The purpose of the Prenatal Repository is to gather tissue samples and data to investigate causes of pregnancy complications, such as delivering a premature or small baby and developing diabetes or hypertension during pregnancy. By collecting this information, researchers can explore the possibility of developing new methods of prenatal diagnosis that may be completed earlier or less invasively to identify women at risk. Additionally, samples and clinical information collected as part of this repository may be used to support future research that aims to further scientific knowledge about prenatal development.
Researchers will ask to include participants' babies (by obtaining information from the babies' medical records) and attempt to enroll the biological father of the babies. The biological fathers willing to participate will be contacted through the mother.
Principal Investigator
John Williams III, MD
Contact
Allynson Novoa
310-423-5860
allynson.novoa@cshs.org