Use of the Perinatal Database and Biologic Tissue Bank at The Perinatology Research Branch (PRB)
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Purpose
The purpose of this application is to request permission to use a bank of biological specimens and clinical information collected by the investigators prior to their joining the intramural program. The samples have been gathered under the sponsorship and approval of the Human Investigations Committees at Yale University, Wayne State University and Pennsylvania Hospital in the United States, the "Sotero del Rio Hospital", the Hospital of the "Universidad de Chile" and the "Universidad Catolica de Chile", in Chile. The investigators have generated a bank of amniotic fluid, maternal blood and urine, and fetal blood obtained at the time of delivery (from the umbilical cord and by cordocentesis), neonate's urine and sonographic examinations of the fetus, including echocardiography, stored on video-tapes. Clinical information with patient identifiers is available for these samples and sonographic examinations.
| Condition |
|---|
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Biological Samples |
| Study Type: | Observational |
| Official Title: | Use of a Perinatal Database and Biologic Tissue Bank at the Perinatology Research Branch (PRB) |
| Estimated Enrollment: | 0 |
| Study Start Date: | July 1995 |
The purpose of this application is to request permission to use a bank of biological specimens and clinical information collected by the investigators prior to their joining the intramural program. The samples have been gathered under the sponsorship and approval of the Human Investigations Committees at Yale University, Wayne State University and Pennsylvania Hospital in the United States, the "Sotero del Rio Hospital", the Hospital of the "Universidad de Chile" and the "Universidad Catolica de Chile", in Chile. The investigators have generated a bank of amniotic fluid, maternal blood and urine, and fetal blood obtained at the time of delivery (from the umbilical cord and by cordocentesis), neonate's urine and sonographic examinations of the fetus, including echocardiography, stored on video-tapes. Clinical information with patient identifiers is available for these samples and sonographic examinations.
Eligibility| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
- Not listed in protocol - samples only.
Contacts and Locations| United States, Maryland | |
| National Institute of Child Health and Human Development (NICHD), 9000 Rockville | |
| Bethesda, Maryland, United States, 20892 | |
| Principal Investigator: | Roberto Romero, M.D. | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00340249 History of Changes |
| Other Study ID Numbers: | 999995040, OH95-CH-N040 |
| Study First Received: | June 19, 2006 |
| Last Updated: | June 13, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institutes of Health Clinical Center (CC):
|
Premature Rupture of the Membranes (PROM) Preterm Delivery In-Utero Fetal Demise Chorioamnionitis Spontaneous Abortion |
ClinicalTrials.gov processed this record on May 16, 2013