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Clinical Trials/KCT0008243
KCT0008243
Recruiting
未知

Evaluation of efficacy and safety using Acellular Dermal Matrix as a Substitute for Middle Hepatic Vein Reconstruction During Living Donor Liver Transplantation, single-center, single-arm, prospective pilot study

Chungnam National University Hospital0 sites10 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Diseases of the digestive system
Sponsor
Chungnam National University Hospital
Enrollment
10
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\) Adults over 19 \~ 70 years old undergoing live liver transplant surgery using the right lobe of the modified liver
  • 2\) GWRW \> 0\.8, MELE Score \< 20, Selected Patients from the Patient Group

Exclusion Criteria

  • 1\) Patients with living liver transplantation using the left lobe of the liver
  • 2\) Patients with living liver transplant using extended right lobe (when MHV reconstruction is not required)
  • 3\) If the right lobe starch section of the liver is dominant and the flow of the reconstructed middle vein is blocked, the patient's
  • If it is expected to have a prognosis
  • 4\) Those who cannot perform both liver CT or liver Doppler tests
  • 5\) Those who are judged unsuitable to participate in this clinical trial by other researchers

Outcomes

Primary Outcomes

Not specified

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