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Autologous Bone Marrow Stem Cells Infusion for the Treatment of Liver Diseases. (ABMSCIFTLD)

Primary Purpose

Liver Diseases

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Autologous bone marrow stem cells infusion
drugs such as Ursodeoxycholic Acid tablets
Sponsored by
Wenzhou Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Liver Diseases focused on measuring liver diseases, Bone Marrow Cell Transplantation

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Definite liver diseases (such as viral hepatitis, autoimmune liver diseases, fatty liver diseases, ect);
  2. Active bone marrow hyperplasia showed by bone marrow biopsy before ABMSCi;
  3. Age between 18 and 60 years;
  4. Abnormal liver function.

Exclusion Criteria:

  1. Enlisted for liver transplantation
  2. Diagnosis of hepatocellular carcinoma or other cancers
  3. Other severe medical disease, and acute infection
  4. pregnant or nursing females,co-infections with HIV ,serious bacterial infection
  5. other vital organ or system dysfunction
  6. with severe complications of liver cirrhosis
  7. hematological disorder

Sites / Locations

  • the First Affiliated Hospital of Wenzhou Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

treatment group: ABMSCi & drugs

control group: drugs

Arm Description

ABMSCi: Autologous bone marrow stem cells infusion drugs such as Ursodeoxycholic Acid tablets(UDCA), each time 150 mg, three times a day orally

drugs such as Ursodeoxycholic Acid tablets(UDCA), each time 150 mg, three times a day orally

Outcomes

Primary Outcome Measures

Change from baseline alanine aminotransferase at 6 months
alanine aminotransferase (ALT)
Change from baseline aspartate aminotransferase at 6 months
aspartate aminotransferase (AST)
Change from baseline total bilirubin at 6 months
total bilirubin (TBil)
Change from baseline direct bilirubin at 6 months
direct bilirubin (DBil)
Change from baseline total bile acid at 6 months
total bile acid (TBA)
Change from baseline albumin at 6 months
albumin (ALB)
Change from baseline prothrombin time at 6 months
prothrombin time (PT),
Change from baseline international normalized ratio at 6 months
international normalized ratio (INR)
Change from baseline white blood cell at 6 months
white blood cell (WBC)
Change from baseline platelet at 6 months
platelet (PLT)

Secondary Outcome Measures

Change from baseline liver density at 6 months
Low density, medium density, high density tested by abdominal B ultrasound/CT/MRI
Change from baseline liver size at 6 months
Enlarged size, normal size, shrunken size tested by abdominal B ultrasound/CT/MRI
Change from baseline spleen thickness at 6 months
tested by abdominal B ultrasound/CT/MRI
Incidence of adverse events that are related to treatment
Postoperative pyrexia, infection, liver cirrhosis, ascites, upper gastrointestinal hemorrhage, malignant tumors of liver and other organs
Number of participants that survive without developing disease
Number of participants that survive with developing disease
Number of participants that die after treatment

Full Information

First Posted
October 17, 2016
Last Updated
October 21, 2016
Sponsor
Wenzhou Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT02943707
Brief Title
Autologous Bone Marrow Stem Cells Infusion for the Treatment of Liver Diseases.
Acronym
ABMSCIFTLD
Official Title
Autologous Bone Marrow Stem Cells Infusion for the Treatment of Liver Diseases.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Unknown status
Study Start Date
October 2016 (undefined)
Primary Completion Date
October 2017 (Anticipated)
Study Completion Date
October 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Wenzhou Medical University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study evaluates the effect of autologous bone marrow stem cells infusion (ABMSCi) therapy for liver diseases.Treatment group will receive ABMSCi and drugs therapy ,while control group will only receive drugs therapy.
Detailed Description
Autologous bone marrow stem cells (ABMSC) mobilization and harvest For harvesting more ABMSC, ABMSC mobilization is induced by recombinant human granulocyte colony stimulating factor (rhGCSF,Gran○R), administered subcutaneously at a dose of 300μg daily for three consecutive days before bone marrow puncture. Bone marrow (160-200ml) of the patients is harvested from both posterior superior iliacs according to standard procedures under local anaesthesia and is collected in a plastic bag containing heparin. Both treatment group and control group receive drugs therapy. ABMSC separation and infusion ABMSC is separated and purified in a class 10,000 clean laboratory. After fat and bony particles are removed by filtration, collected cells are moved to a cell-processing device. The reagents adopt the method of negative cells collection. Take the cells which intended to remove as target cells, and carry out the removal step-by-step. On the basis of this method, red blood cells, blood platelets, blood plasma will be completely removed with part of white cells and lymphocytes being remarkably removed as well while all the stem cells / progenitor cells are being well retained. The nucleated cell (white blood cell) count of final ABMSC is measured by an automated complete blood count instrument and flow cytometry analysis. The number of mononuclear cells is counted manually under a microscope by Wright-Giemsa stain method. Cell differentiation factor 34(CD34) positive cells were determined by flow cytometry analysis. The time of ABMSC separation and purification is 2.5-3 hours. ABMSC is added to 10 ml saline and well mixed by shaking the vial gently. The catheter is pushed to reach the proper hepatic artery. The diameter of the catheter is 1.4mm, it is thin enough to easily been inserted to right gastric artery . The mixture of saline and ABMSC is infused into proper hepatic artery at uniform speed for about two minutes. The catheter is removed after the ABMSCi. Statistical analysis - Categorical data are presented as absolute values and percentages, whereas continuous data are summarized as mean and Standard Deviation. Statistical analysis was performed using t-test for paired or unpaired samples. Time courses of measurements of liver function parameters were analyzed by repeated-measures ANOVA. The analysis is performed using the Statistic Package for Social Science (SPSS). All statistical analysis is based on two-tailed hypothesis tests with a significance level of p< 0.05.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Diseases
Keywords
liver diseases, Bone Marrow Cell Transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
treatment group: ABMSCi & drugs
Arm Type
Experimental
Arm Description
ABMSCi: Autologous bone marrow stem cells infusion drugs such as Ursodeoxycholic Acid tablets(UDCA), each time 150 mg, three times a day orally
Arm Title
control group: drugs
Arm Type
Active Comparator
Arm Description
drugs such as Ursodeoxycholic Acid tablets(UDCA), each time 150 mg, three times a day orally
Intervention Type
Procedure
Intervention Name(s)
Autologous bone marrow stem cells infusion
Other Intervention Name(s)
ABMSCi
Intervention Description
Autologous bone marrow stem cells are infused into proper hepatic artery
Intervention Type
Drug
Intervention Name(s)
drugs such as Ursodeoxycholic Acid tablets
Other Intervention Name(s)
UDCA
Intervention Description
Ursodeoxycholic Acid tablets(UDCA), each time 150 mg, three times a day orally
Primary Outcome Measure Information:
Title
Change from baseline alanine aminotransferase at 6 months
Description
alanine aminotransferase (ALT)
Time Frame
baseline and 6 months after treatment
Title
Change from baseline aspartate aminotransferase at 6 months
Description
aspartate aminotransferase (AST)
Time Frame
baseline and 6 months after treatment
Title
Change from baseline total bilirubin at 6 months
Description
total bilirubin (TBil)
Time Frame
baseline and 6 months after treatment
Title
Change from baseline direct bilirubin at 6 months
Description
direct bilirubin (DBil)
Time Frame
baseline and 6 months after treatment
Title
Change from baseline total bile acid at 6 months
Description
total bile acid (TBA)
Time Frame
baseline and 6 months after treatment
Title
Change from baseline albumin at 6 months
Description
albumin (ALB)
Time Frame
baseline and 6 months after treatment
Title
Change from baseline prothrombin time at 6 months
Description
prothrombin time (PT),
Time Frame
baseline and 6 months after treatment
Title
Change from baseline international normalized ratio at 6 months
Description
international normalized ratio (INR)
Time Frame
baseline and 6 months after treatment
Title
Change from baseline white blood cell at 6 months
Description
white blood cell (WBC)
Time Frame
baseline and 6 months after treatment
Title
Change from baseline platelet at 6 months
Description
platelet (PLT)
Time Frame
baseline and 6 months after treatment
Secondary Outcome Measure Information:
Title
Change from baseline liver density at 6 months
Description
Low density, medium density, high density tested by abdominal B ultrasound/CT/MRI
Time Frame
baseline and 6 months after treatment
Title
Change from baseline liver size at 6 months
Description
Enlarged size, normal size, shrunken size tested by abdominal B ultrasound/CT/MRI
Time Frame
baseline and 6 months after treatment
Title
Change from baseline spleen thickness at 6 months
Description
tested by abdominal B ultrasound/CT/MRI
Time Frame
baseline and 6 months after treatment
Title
Incidence of adverse events that are related to treatment
Description
Postoperative pyrexia, infection, liver cirrhosis, ascites, upper gastrointestinal hemorrhage, malignant tumors of liver and other organs
Time Frame
baseline and 6 months after treatment
Title
Number of participants that survive without developing disease
Time Frame
12 months after treatment
Title
Number of participants that survive with developing disease
Time Frame
12 months after treatment
Title
Number of participants that die after treatment
Time Frame
12 months after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Definite liver diseases (such as viral hepatitis, autoimmune liver diseases, fatty liver diseases, ect); Active bone marrow hyperplasia showed by bone marrow biopsy before ABMSCi; Age between 18 and 60 years; Abnormal liver function. Exclusion Criteria: Enlisted for liver transplantation Diagnosis of hepatocellular carcinoma or other cancers Other severe medical disease, and acute infection pregnant or nursing females,co-infections with HIV ,serious bacterial infection other vital organ or system dysfunction with severe complications of liver cirrhosis hematological disorder
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
yongping chen
Phone
8613505777281
Email
13505777281@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
lanman xu
Phone
8613587646315
Email
13587646315@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
yongping chen
Organizational Affiliation
First Affiliated Hospital of Wenzhou Medical University
Official's Role
Study Chair
Facility Information:
Facility Name
the First Affiliated Hospital of Wenzhou Medical University
City
Wenzhou
State/Province
Zhejiang
ZIP/Postal Code
325000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
yongping chen
Phone
8613505777281
Email
13505777281@163.com
First Name & Middle Initial & Last Name & Degree
lanman xu
Phone
8613587646315
Email
13587646315@163.com
First Name & Middle Initial & Last Name & Degree
yongping chen, MD
First Name & Middle Initial & Last Name & Degree
lanman xu, PhD
First Name & Middle Initial & Last Name & Degree
dazhi chen, MD
First Name & Middle Initial & Last Name & Degree
minghua zheng, PhD
First Name & Middle Initial & Last Name & Degree
keqing shi, MD
First Name & Middle Initial & Last Name & Degree
yu huang, MD
First Name & Middle Initial & Last Name & Degree
faling wu, MD
First Name & Middle Initial & Last Name & Degree
ruicong chen, MD
First Name & Middle Initial & Last Name & Degree
yunlei xiao, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
25861263
Citation
Ma XR, Tang YL, Xuan M, Chang Z, Wang XY, Liang XH. Transplantation of autologous mesenchymal stem cells for end-stage liver cirrhosis: a meta-analysis based on seven controlled trials. Gastroenterol Res Pract. 2015;2015:908275. doi: 10.1155/2015/908275. Epub 2015 Mar 15.
Results Reference
background
PubMed Identifier
24942592
Citation
Xu L, Gong Y, Wang B, Shi K, Hou Y, Wang L, Lin Z, Han Y, Lu L, Chen D, Lin X, Zeng Q, Feng W, Chen Y. Randomized trial of autologous bone marrow mesenchymal stem cells transplantation for hepatitis B virus cirrhosis: regulation of Treg/Th17 cells. J Gastroenterol Hepatol. 2014 Aug;29(8):1620-8. doi: 10.1111/jgh.12653.
Results Reference
result
PubMed Identifier
21608000
Citation
Peng L, Xie DY, Lin BL, Liu J, Zhu HP, Xie C, Zheng YB, Gao ZL. Autologous bone marrow mesenchymal stem cell transplantation in liver failure patients caused by hepatitis B: short-term and long-term outcomes. Hepatology. 2011 Sep 2;54(3):820-8. doi: 10.1002/hep.24434. Epub 2011 Jul 14.
Results Reference
result
PubMed Identifier
26977164
Citation
Deng Q, Cai T, Zhang S, Hu A, Zhang X, Wang Y, Huang J. Autologous Peripheral Blood Stem Cell Transplantation Improves Portal Hemodynamics in Patients with Hepatitis B Virus-related Decompensated Cirrhosis. Hepat Mon. 2015 Dec 20;15(12):e32498. doi: 10.5812/hepatmon.32498. eCollection 2015 Dec.
Results Reference
result
PubMed Identifier
26659833
Citation
Mohamadnejad M, Vosough M, Moossavi S, Nikfam S, Mardpour S, Akhlaghpoor S, Ashrafi M, Azimian V, Jarughi N, Hosseini SE, Moeininia F, Bagheri M, Sharafkhah M, Aghdami N, Malekzadeh R, Baharvand H. Intraportal Infusion of Bone Marrow Mononuclear or CD133+ Cells in Patients With Decompensated Cirrhosis: A Double-Blind Randomized Controlled Trial. Stem Cells Transl Med. 2016 Jan;5(1):87-94. doi: 10.5966/sctm.2015-0004. Epub 2015 Dec 10.
Results Reference
result
PubMed Identifier
25445618
Citation
Chen Y, Chen S, Liu LY, Zou ZL, Cai YJ, Wang JG, Chen B, Xu LM, Lin Z, Wang XD, Chen YP. Mesenchymal stem cells ameliorate experimental autoimmune hepatitis by activation of the programmed death 1 pathway. Immunol Lett. 2014 Dec;162(2 Pt B):222-8. doi: 10.1016/j.imlet.2014.10.021. Epub 2014 Oct 28.
Results Reference
result

Learn more about this trial

Autologous Bone Marrow Stem Cells Infusion for the Treatment of Liver Diseases.

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