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Pilot Study Freeze and Transport Immune Cells - Article


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Tetanus

Lockjaw 




Clinical Trial: Pilot Study Freeze and Transport Immune Cells

This study is no longer recruiting patients.

Sponsored by: National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by: National Institute of Allergy and Infectious Diseases (NIAID)
ClinicalTrials.gov Identifier: NCT00138268

Purpose

To evaluate and standardize umbilical cord specimen collection and laboratory procedures to evaluate cellular and serological immune responses in neonates and young infants
Condition
Diphtheria
Hepatitis B
Pertussis
Poliomyelitis
Tetanus

MedlinePlus related topics:  Bacterial Infections;   Bronchitis;   Diphtheria;   Hepatitis B;   Polio and Post-Polio Syndrome;   Respiratory Diseases;   Tetanus

Study Type: Observational
Study Design: Screening, Convenience Sample, Prospective Study

Official Title: Pilot Study to Optimize and Standardize Umbilical Cord Blood Collection and the Isolation, Freezing and Transportation of Cells for Studies of Cellular Immune Responses to Immunization

Further Study Details: 

Expected Total Enrollment:  12

Study completion: December 2004
Last follow-up: February 2005

To evaluate: 1) The procedures for obtaining umbilical cord blood; 2) the methods for ensuring immune cell viability, freezing, and shipping; 3) the conditions for optimization of immune cell isolation procedures.

Eligibility

Criteria

Inclusion Criteria:

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.

Exclusion Criteria:

Location Information


California
      UCLA Center For Vaccine Research, Torrance,  California,  90502,  United States

More Information

Study ID Numbers:  03-236
Last Updated:  September 12, 2005
Record first received:  August 26, 2005
ClinicalTrials.gov Identifier:  NCT00138268
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-09-13

Resources



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November 29, 2009



Page Updated: October 15, 2009
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