- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00234624
Hepatic Hemodynamic Changes and Simulation in Living-Related Liver Transplantation
October 5, 2005 updated by: National Taiwan University Hospital
Hepatic Hemodynamic Changes and Simulation Before /After Living-Related Liver Transplantation in Donors/Recipients
This 1-year project is intended to study the hemodynamic changes of poratal and hepatic artery during living related liver transplantation.
We hypothesize that after right hepatectomy for living related liver transplatation, portal vein overflow will change the remnant liver contour and result in liver hyperplasia.
Study Overview
Status
Unknown
Conditions
Detailed Description
We use CT as tools to reconstruct 3D images of portal vein and hepatic artery before and one month after operation.
The images are transferred to CAD and computer simulation is performed.
Study Type
Observational
Enrollment
10
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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Taipei, Taiwan, 100
- Recruiting
- NTUH
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Sub-Investigator:
- Cheng-Maw Ho, MD
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Contact:
- Cheng-Maw Ho, MD
- Phone Number: 9801914 +886-2-23123456
- Email: miningho@ntu.edu.tw
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Contact:
- Po-Huang Lee, PhD
- Phone Number: 5104 +886-2-23123456
- Email: pohuang@ha.mc.ntu.edu.tw
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Principal Investigator:
- Po-Huang Lee, PhD
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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
21 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria: - Informed adult-to adult living donor underwent right lobectomy
Exclusion Criteria:
- no written informed contents
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?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Po-Huang Lee, PhD, NTUH
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, 2005
Study Registration Dates
First Submitted
October 5, 2005
First Submitted That Met QC Criteria
October 5, 2005
First Posted (Estimate)
October 7, 2005
Study Record Updates
Last Update Posted (Estimate)
October 7, 2005
Last Update Submitted That Met QC Criteria
October 5, 2005
Last Verified
September 1, 2005
More Information
Terms related to this study
Other Study ID Numbers
- 9461700821
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.