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microRNA Profile in Umbilical Cord Blood NK Cells

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified September 2008 by National Taiwan University Hospital.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00751569
First Posted: September 12, 2008
Last Update Posted: September 12, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
National Taiwan University Hospital
  Purpose
Umbilical cords contain immature blood cells, including a group of lymphocytes, that are important in the so-called natural immunity. We want to study the cytokine levels in umbilical cord NK cells and its regulation a family of newly identified small RNAs (microRNAs).

Condition Intervention
Pregnant Women Other: blood donation

Study Type: Observational
Official Title: microRNA Profile in Umbilical Cord Blood NK Cells

Further study details as provided by National Taiwan University Hospital:

Biospecimen Retention:   Samples With DNA
Umbilical cord blood

Estimated Enrollment: 5
Study Start Date: September 2008
Estimated Study Completion Date: September 2009
Groups/Cohorts Assigned Interventions
A1
A group of 3 to 5 pregnant women as donors for umbilical cord blood
Other: blood donation
obtaining cord blood
Other Name: cord blood donation

Detailed Description:
Our preliminary data pointed to the possibility of cytokine regulation by microRNAs in NK lymphoma and NK lymphoma cell lines. We want to use umbilical cord blood as controls for the biological significance in normal NK cell development.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
normal pregnant women
Criteria

Inclusion Criteria:

  • Normal pregnant women

Exclusion Criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00751569


Contacts
Contact: Chung-wu LIn 02-23123456 ext 65454 chungwulin@yahoo.com

Locations
Taiwan
National Taiwan University Hospital Recruiting
Taipei, Taiwan
Contact: Chung-Wu Lin    02-23123456 ext 65454    chungwulin@yahoo.com   
Principal Investigator: Chung-Wu Lin         
Sponsors and Collaborators
National Taiwan University Hospital
Investigators
Principal Investigator: Chung-Wu Lin National Taiwan University
  More Information

Responsible Party: Chung-Wu Lin, national Taiwan University Hospital
ClinicalTrials.gov Identifier: NCT00751569     History of Changes
Other Study ID Numbers: 200808006R
First Submitted: September 10, 2008
First Posted: September 12, 2008
Last Update Posted: September 12, 2008
Last Verified: September 2008

Keywords provided by National Taiwan University Hospital:
umbilical cord blood