SALT in Adolescents With End-stage Liver Disease

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age7-18
SponsorRenJi Hospital

About this trial

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.

Eligibility criteria

Qualifiers

Age 7-18 years old;

Patients with end-stage liver disease cannot obtain sufficient donor liver volume through conventional living donor liver transplantation;

The general condition is good and can tolerate the follow-up operation plan;

Guardians and children (over 14 years old) sign the informed consent.

Disqualifiers

Uncorrectable cardiopulmonary disease with excessive surgical risk

Anatomical abnormalities precluding liver transplantation

Patients with primary or secondary hepatic malignancies

Patients with genetic metabolic diseases and their complications that cannot be completely cured by liver transplantation

Trial design

Treatments tested in this trial

  • sequential adolesent left lateral lobe liver transplantation (SALT)

Treatment groups

20 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators