Human Umbilical Cord-mesenchymal Stem Cells Via Different Transplantation Routes in ESLD

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorGeneral Hospital of Shenyang Military Region

About this trial

Stem cells are non-terminal cells that can self renew and replicate through symmetric or asymmetric division, with the potential to differentiate into different types of cells and tissues. Multiple studies have shown that human umbilical cord mesenchymal stem cell has good safety and effectiveness in improving acute or chronic liver injury.

Stem cell therapy for end-stage liver disease (ESLD) can be administered through various routes, among which hepatic artery and peripheral vein infusions are the most commonly used in clinical practice. The efficacy of hepatic artery infusion appears to be greater than that of peripheral vein infusion.

Eligibility criteria

Qualifiers

18-80 years old

End-stage liver disease

Signed informed consent

Disqualifiers

Tumours of the liver or other organs

Liver transplantation recipients

Acute myocardial infarction, acute heart failure, type I and type II respiratory failure, pulmonary embolism, acute cerebral infarction, acute cerebral haemorrhage and other serious cardiopulmonary diseases

Other diseases that may seriously affect the survival

Trial design

Treatments tested in this trial

  • Infusion of umbilical cord-mesenchymal stem cells through peripheral veins
  • Infusion of umbilical cord-mesenchymal stem cells through hepatic artery

Treatment groups

32 Participants
are divided into 2 treatment groups