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Establishment of Vascular Permeability Model for Research Purpose by Human Umbilical Vascular Endothelial 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 June 2011 by Kaohsiung Medical University Chung-Ho Memorial Hospital.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01261195
First Posted: December 16, 2010
Last Update Posted: August 17, 2011
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:
Kaohsiung Medical University Chung-Ho Memorial Hospital
  Purpose
HUVEC primary cells for researches about the relation between plasma leakage and infections.

Condition
Healthy People

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Establishment of Vascular Permeability Model for Research Purpose by Human

Further study details as provided by Kaohsiung Medical University Chung-Ho Memorial Hospital:

Biospecimen Retention:   Samples With DNA
the umbilical cord

Estimated Enrollment: 60
Study Start Date: March 2010
Estimated Study Completion Date: December 2011
Estimated Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
Detailed Description:
This study is going to collect HUVEC primary cells to set up an in vitro model for researches about the relation between plasma leakage and infections.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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

Inclusion Criteria:

  • healthy pregnant women
  • would like to join this study

Exclusion Criteria:

  • venereal disease
  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): NCT01261195


Contacts
Contact: Jessie Jou, Assistant 886-7-3121101 ext 6361 r93445113@gmail.com

Locations
Taiwan
Kaohsiung Medical University Chung-Ho Memorial Hospital Recruiting
Kaohsiung, Taiwan, 807
Contact: Jessie Jou, Assistant    886-7-3121101 ext 6361    r93445113@gmail.com   
Sponsors and Collaborators
Kaohsiung Medical University Chung-Ho Memorial Hospital
Investigators
Principal Investigator: Jih-Jin Tsai, Doctor KMUH Tropical Medicine Center
  More Information

Responsible Party: Jih-Jin Tsai, Kaohsiung Medical University Chung-Ho Memorial Hospital
ClinicalTrials.gov Identifier: NCT01261195     History of Changes
Other Study ID Numbers: KMUH-IRB-990030
First Submitted: December 14, 2010
First Posted: December 16, 2010
Last Update Posted: August 17, 2011
Last Verified: June 2011