Clinical Trial Details
— Status: Not yet recruiting
Administrative data
NCT number |
NCT06069050 |
Other study ID # |
LY2023-184-C |
Secondary ID |
|
Status |
Not yet recruiting |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
October 20, 2023 |
Est. completion date |
March 30, 2027 |
Study information
Verified date |
October 2023 |
Source |
RenJi Hospital |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
End-stage liver disease is synonymous with advanced liver disease, liver failure, and
decompensated cirrhosis, and their disease progression is generally irreversible. Unlike
other end-stage diseases, liver transplantation is a definitive and potentially curative
treatment for ESLD. However, due to clinical and social factors such as the shortage of donor
livers, the number of patients who can be transplanted is far less than the number of waiting
patients. About 14% of patients die each year while waiting, and about 10% of patients are
too sick to be transplanted. Although changes in organ allocation policies and popularization
of living donor liver transplantation have significantly reduced the waiting time and
mortality of infant recipients under 2 years old. Pre-transplant mortality in children older
than 6 years remains high. Therefore, expanding the donor liver pool is an urgent need to
treat patients with adolescent end-stage liver disease (AESLD). In 2015, Norwegian scholars
proposed a new surgical method, that is, resection and partial liver segment (2-3 segment)
transplantation combined with delayed total hepatectomy can greatly alleviate the shortage of
liver donors in the above patients.Based on the experience of clinical operation, our center
proposes and designs the clinical research of sequential adolescent left lateral lobe liver
transplantation (SALT) for the treatment of AESLD. On the basis of RAPID, the safety and
efficacy of sequential juvenile left lateral lobe liver transplantation were evaluated for
the above patients.
Description:
Cirrhosis is an irreversible advanced stage of chronic progressive liver disease
characterized by structural deformation of the liver and the formation of regenerative
nodules. Those with complications are classified as decompensated cirrhosis, including
variceal bleeding, ascites, spontaneous bacterial peritonitis, hepatocellular carcinoma
(HCC), hepatorenal syndrome, or hepatopulmonary syndrome. These complications are the leading
cause of death in patients with cirrhosis. End-stage liver disease is synonymous with
advanced liver disease, liver failure, and decompensated cirrhosis, and their disease
progression is generally irreversible. Unlike other end-stage diseases, liver transplantation
is a definitive and potentially curative treatment for ESLD. However, due to clinical and
social factors such as the shortage of donor livers, the number of patients who can be
transplanted is far less than the number of waiting patients. About 14% of patients die each
year while waiting, and about 10% of patients are too sick to be transplanted. Although
changes in organ allocation policies and popularization of living donor liver transplantation
have significantly reduced the waiting time and mortality of infant recipients under 2 years
old. Pre-transplant mortality in children older than 6 years remains high. Therefore,
expanding the donor liver pool is an urgent need to treat patients with adolescent end-stage
liver disease (AESLD). In 2015, a new surgical method was proposed by Norwegian scholars.
Therefore, expanding the donor liver pool is an urgent need to treat patients with adolescent
end-stage liver disease (AESLD). In 2015, Norwegian scholars proposed a new surgical method,
that is, resection and partial liver segment 2-3 transplantation with delayed total
hepatectomy (RAPID). This approach allows transplantation of the left liver (segments 2+3) to
an adult recipient, while the remaining enlarged right hemi-liver is transplanted to another
adult recipient. Recipients who received right-hemi-liver transplantation had a similar
prognosis compared with those who received whole-liver transplantation. Therefore, if the
RAPID technique is confirmed to be feasible, it can greatly alleviate the shortage of liver
donors. In addition to cadaver sources, living adult donors can also be considered as the
source of liver donors. A smaller left lateral lobe donor liver also places less burden on
the donor than a left or right hemiliver.
To sum up, our center proposed and designed a clinical study of sequential adolescent left
lateral lobe liver transplantation (SALT) in the treatment of AESLD patients based on
clinical surgical experience. On the basis of RAPID operation, the overall survival rate of
SALT in AESLD patients was evaluated.