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Umbilical Cord Mesenchymal Stem Cells Transplantation Combined With Plasma Exchange for Patients With Liver Failure

Primary Purpose

Liver Failure

Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
Conventional plus UC-MSC treatment
Conventional plus PE treatment
Conventional plus UC-MSC and PE therapy
Conventional treatment
Sponsored by
Third Affiliated Hospital, Sun Yat-Sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Liver Failure focused on measuring mesenchymal stem cells, plasma exchange, liver failure, hepatitis B virus

Eligibility Criteria

16 Years - 65 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Written informed consent
  • Acute-on-Chronic liver failure caused by hepatitis B virus
  • Model for End-Stage Liver Disease (MELD) <30

Exclusion Criteria:

  • Liver failure caused by other reasons, such as autoimmune diseases, alcohol, drug and so on
  • History of severe hepatic encephalopathy or variceal bleeding during the last two months before enrollment
  • Severe problems in other vital organs(e.g. the heart, renal or lungs)
  • Severe bacteria infection
  • Tumor on ultrasonography, CT or MRI examination
  • Pregnant or lactating women

Sites / Locations

  • Department of Infectious Diseases, The Third Affliated Hospital of Sun Yat-sen UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Conventional treatment

Conventional plus UC-MSC treatment

Conventional plus PE treatment

Conventional plus UC-MSC and PE therapy

Arm Description

Participants will receive conventional treatment and then be followed until the week 48 study visit.

Participants will receive conventional treatment plus a dose of UC-MSC and then be followed until the week 48 study visit.

Participants will receive conventional treatment plus plasma exchange and then be followed until the week 48 study visit.

Participants will receive conventional treatment plus umbilical cord mesenchymal stem cells transplantation combined with plasma exchange. Participants will then be followed until the week 48 study visit.

Outcomes

Primary Outcome Measures

Survival rate and time

Secondary Outcome Measures

Improve biochemical indexes [alanine aminotransferase (ALT), albumin (ALB), total bilirubin (TBIL), prothrombin time (PT), INR and so on]
The clinical symptom improvement [including appetite, debilitation, abdominal distension, edema of lower limbs, et al]
Liver function evaluation using Child-Pugh score and MELD score
Immune function improvement [including Th1/Th2]
The occurrence of complications [including body temperature, tetter and allergy]
Incidence of hepatocellular carcinoma

Full Information

First Posted
November 4, 2012
Last Updated
February 27, 2013
Sponsor
Third Affiliated Hospital, Sun Yat-Sen University
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1. Study Identification

Unique Protocol Identification Number
NCT01724398
Brief Title
Umbilical Cord Mesenchymal Stem Cells Transplantation Combined With Plasma Exchange for Patients With Liver Failure
Official Title
Safety and Efficacy of Human Umbilical Cord Mesenchymal Stem Cells Transplantation Combined With Plasma Exchange for Patients With Acute-on-Chronic Liver Failure Caused by Hepatitis B Virus (HBV)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2013
Overall Recruitment Status
Unknown status
Study Start Date
November 2012 (undefined)
Primary Completion Date
March 2015 (Anticipated)
Study Completion Date
March 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Third Affiliated Hospital, Sun Yat-Sen University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Liver failure (LF) is a dramatic clinical syndrome with massive necrosis of liver cells. Although liver transplantation provides an option to cure patients suffering with LF, lack of donors, postoperative complications, especially rejection, and high cost limit its application. Previous study showed that bone marrow derived mesenchymal stem cells (BM-MSCs) the novel and promising therapeutic strategy, BM-MSCs can replace hepatocytes in injured liver, and effectively rescue experimental liver failure and contribute to liver regeneration. Plasma exchange (PE) can improve internal environment by removing endotoxin, it helps the liver regeneration and functional recovery and make UC-MSC differentiation into hepatocyte like cells, and exert immunomodulatory function. In this study, safety and efficacy of human umbilical cord mesenchymal stem cells (UC-MSCs) transplantation combined with plasma exchange (PE) for patients with liver failure caused by hepatitis B Virus will be evaluated.
Detailed Description
To investigate safety and efficacy of human umbilical cord mesenchymal stem cells (UC-MSCs) transplantation combined with plasma exchange (PE) for patients with liver failure caused by hepatitis B virus.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Failure
Keywords
mesenchymal stem cells, plasma exchange, liver failure, hepatitis B virus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conventional treatment
Arm Type
Experimental
Arm Description
Participants will receive conventional treatment and then be followed until the week 48 study visit.
Arm Title
Conventional plus UC-MSC treatment
Arm Type
Experimental
Arm Description
Participants will receive conventional treatment plus a dose of UC-MSC and then be followed until the week 48 study visit.
Arm Title
Conventional plus PE treatment
Arm Type
Experimental
Arm Description
Participants will receive conventional treatment plus plasma exchange and then be followed until the week 48 study visit.
Arm Title
Conventional plus UC-MSC and PE therapy
Arm Type
Experimental
Arm Description
Participants will receive conventional treatment plus umbilical cord mesenchymal stem cells transplantation combined with plasma exchange. Participants will then be followed until the week 48 study visit.
Intervention Type
Other
Intervention Name(s)
Conventional plus UC-MSC treatment
Intervention Description
Received conventional treatment and umbilical cord mesenchymal stem cells transplantation by peripheral vein slowly for 30minutes. (1×105/Kg, once a week, 4 times).
Intervention Type
Other
Intervention Name(s)
Conventional plus PE treatment
Intervention Description
Received conventional treatment plus 2000 milliliter plasma exchange (every 3 days, 3 times).
Intervention Type
Other
Intervention Name(s)
Conventional plus UC-MSC and PE therapy
Intervention Description
Received conventional treatment plus 2000 milliliter plasma exchange (every 3 days, 3 times). Meantime taken i.v umbilical cord mesenchymal stem cells transplantation slowly for 30minutes (1×105/Kg, once a week, 4 times), the first two times is taken after plasma exchange.
Intervention Type
Other
Intervention Name(s)
Conventional treatment
Intervention Description
Received conventional treatment including antiviral drugs, lowering aminotransferase and jaundice medicine.
Primary Outcome Measure Information:
Title
Survival rate and time
Time Frame
48 weeks
Secondary Outcome Measure Information:
Title
Improve biochemical indexes [alanine aminotransferase (ALT), albumin (ALB), total bilirubin (TBIL), prothrombin time (PT), INR and so on]
Time Frame
24 weeks after treatment
Title
The clinical symptom improvement [including appetite, debilitation, abdominal distension, edema of lower limbs, et al]
Time Frame
24 weeks after treatment
Title
Liver function evaluation using Child-Pugh score and MELD score
Time Frame
24 weeks after treatment
Title
Immune function improvement [including Th1/Th2]
Time Frame
24 weeks after treatment
Title
The occurrence of complications [including body temperature, tetter and allergy]
Time Frame
Between 0 to 8 hours after UC-MSCs transfusion
Title
Incidence of hepatocellular carcinoma
Time Frame
48 weeks after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Written informed consent Acute-on-Chronic liver failure caused by hepatitis B virus Model for End-Stage Liver Disease (MELD) <30 Exclusion Criteria: Liver failure caused by other reasons, such as autoimmune diseases, alcohol, drug and so on History of severe hepatic encephalopathy or variceal bleeding during the last two months before enrollment Severe problems in other vital organs(e.g. the heart, renal or lungs) Severe bacteria infection Tumor on ultrasonography, CT or MRI examination Pregnant or lactating women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhi-Liang Gao, Professor
Phone
86-20-85252373
Email
zhilianggao@21cn.com
First Name & Middle Initial & Last Name or Official Title & Degree
Hong-Liang He, Master
Phone
86-20-85253372
Email
hehongliang0925@sina.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhi-Liang Gao, Doctor
Organizational Affiliation
The Third Affliated Hospital of Sun Yat-sen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Infectious Diseases, The Third Affliated Hospital of Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510630
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhi-Liang Gao, Professor
Phone
86-20-85252373
Email
zhilianggao@21cn.com
First Name & Middle Initial & Last Name & Degree
Hong-Liang He, Master
Phone
86-20-85253372
Email
hehongliang0925@sina.com
First Name & Middle Initial & Last Name & Degree
Zhi-Liang Gao, Professor

12. IPD Sharing Statement

Citations:
PubMed Identifier
30863450
Citation
Xu WX, He HL, Pan SW, Chen YL, Zhang ML, Zhu S, Gao ZL, Peng L, Li JG. Combination Treatments of Plasma Exchange and Umbilical Cord-Derived Mesenchymal Stem Cell Transplantation for Patients with Hepatitis B Virus-Related Acute-on-Chronic Liver Failure: A Clinical Trial in China. Stem Cells Int. 2019 Feb 4;2019:4130757. doi: 10.1155/2019/4130757. eCollection 2019.
Results Reference
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Umbilical Cord Mesenchymal Stem Cells Transplantation Combined With Plasma Exchange for Patients With Liver Failure

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