Pilot Study Freeze and Transport Immune Cells
Completed
Conditions studied: Diphtheria, Hepatitis B, Pertussis, Poliomyelitis, Tetanus
In brief
To evaluate and standardize umbilical cord specimen collection and laboratory procedures to evaluate cellular and serological immune responses in neonates and young infants
Key facts
- Study ID
- NCT00138268
- Run by
- National Institute of Allergy and Infectious Diseases (NIAID)
- People needed
- 12
- Expected to finish
- 2005-02-01
- Last updated by the study team
- 2010-08-27
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- For the portion of the pilot study conducted at the UCLA CVR, an umbilical cord blood sample will be obtained from approximately 8 to 12 healthy pregnant women who are delivering neonates at the Obstetrical delivery ward of Harbor- UCLA Medical Center. Informed consent will not be obtained because the blood will be obtained after delivery from a clamped umbilical cord attached to the placenta (afterbirth) that otherwise would be discarded.
You may not qualify if…
- A cord blood sample will not be collected from women who have requested special arrangements for a cord blood registry service.
Where it is running
- UCLA Center For Vaccine Research — Torrance, California, United States
Full record on ClinicalTrials.gov
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