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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01205802 |
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Date of registration:
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20/09/2010 |
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Primary sponsor: |
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Public title:
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Usability of Ringed Polytetrafluoroethylene Graft for Venous Vascular Reconstruction of Living Donor Liver Transplantation
MHVLDLT |
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Scientific title:
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Prospective Study on Usability of Ringed Polytetrafluoroethylene Graft for Venous Vascular Reconstruction of Living Donor Liver Transplantation |
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Date of first enrolment:
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August 2010 |
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Target sample size:
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200 |
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Recruitment status: |
Enrolling by invitation |
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URL:
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http://clinicaltrials.gov/show/NCT01205802 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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Countries of recruitment
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Korea, Republic of
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Living donor liver transplantation requiring MHV reconstruction
Exclusion Criteria:
- Living donor liver transplantation not requiring MHV reconstruction
Age minimum:
N/A
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Patency, Hepatic Venous Congestion
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Intervention(s)
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Procedure: MHV reconstruction
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Primary Outcome(s)
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Patency of the reconstructed MHV
[Time Frame: Follow-up for 1 year]
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Secondary ID(s)
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MHV_Goretex_LDLT
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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