Human Umbilical Cord-Mesenchymal Stem Cells for Hepatic Cirrhosis

Shenzhen Hornetcorn Biotechnology

Status and phase

Unknown

Phase 1

Conditions

Hepatic Cirrhosis

Treatments

Biological: Human umbilical cord mesenchymal stem cells

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT02652351

HYK-hepatic cirrhosis

Details and patient eligibility

About

The purpose of this study is to evaluate the safety and efficacy of human umbilical cord mesenchymal stem cell(hUC-MSC) for Hepatic Cirrhosis.

Full description

Human umbilical cord mesenchymal stem cells exhibit the potential to differentiate into mature cells typical of several tissues, which have been confirmed in in vivo and in vitro experiments. There have been few clinical reports describing umbilical cord mesenchymal stem cells for treatment of Hepatic Cirrhosis.

To investigate the effects of hUC-MSC treatment for Hepatic Cirrhosis, 20 patients with Hepatic Cirrhosis will be enrolled and receive 4 times of hUC-MSC transplantation.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

The patient who have signed the informed consent document;
Clinical, radiological, or biochemical evidence of liver cirrhosis.

Exclusion criteria

Pregnant women or lactating mothers;
Patients who have received any anti-inflammatory drugs including herb-drug within 14 days;
Patients who received any drug by intra-articular injection for treatment within 2 months prior to this enrollment;
Patients with positive human immunodeficiency (HIV) at screening indicative of current of pass infection;
Abnormal blood coagulation, combine other tumor or special condition;
Patients who had participated in other clinical trials within three months prior to this study.