- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00751569
microRNA Profile in Umbilical Cord Blood NK Cells
September 11, 2008 updated by: National Taiwan University Hospital
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).
Study Overview
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.
Study Type
Observational
Enrollment (Anticipated)
5
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Taipei, Taiwan
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Chung-Wu Lin
- Phone Number: 65454 02-23123456
- Email: chungwulin@yahoo.com
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Principal Investigator:
- Chung-Wu Lin
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
normal pregnant women
Description
Inclusion Criteria:
- Normal pregnant women
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
A1
A group of 3 to 5 pregnant women as donors for umbilical cord blood
|
obtaining cord blood
Other Names:
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Chung-Wu Lin, National Taiwan University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2008
Study Completion (Anticipated)
September 1, 2009
Study Registration Dates
First Submitted
September 10, 2008
First Submitted That Met QC Criteria
September 11, 2008
First Posted (Estimate)
September 12, 2008
Study Record Updates
Last Update Posted (Estimate)
September 12, 2008
Last Update Submitted That Met QC Criteria
September 11, 2008
Last Verified
September 1, 2008
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 200808006R
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.