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Combination of Autologous MSC and HSC Infusion in Patients With Decompensated Cirrhosis

Primary Purpose

Cirrhosis, Liver

Status
Completed
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
CD 34 and MSC infusion
Standard of care for Cirrhosis management
Sponsored by
Asian Institute of Gastroenterology, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cirrhosis, Liver focused on measuring Mesenchymal Stem Cell, Hematopoetic Stem cell, Autologous transfusion

Eligibility Criteria

20 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age between 20-70 years
  • Clinically diagnosed for hepatic cirrhosis having a Child Pugh score of B or MELD >10 but below 20
  • Not willing for immediate liver transplantation either due to lack of donor tissue or financial issues
  • Platelet count of > 80,000 and INR <1.6
  • Life expectancy of at least 3 months based on MELD score and Child Pugh Score
  • Ability to give informed consent

Exclusion Criteria:

  • Age less than 20 or more than 70 years
  • Have liver tumors or history of any other cancer
  • Pregnant or lactating women
  • Patients with hepato-renal syndrome and acute kidney injury (Any creatinine > 1.6 will be excluded)
  • Evidence of ongoing sepsis - as per Surviving sepsis guideline
  • Recent gastrointestinal bleeding or spontaneous bacterial peritonitis (within last one month)
  • Any HIV positive patients
  • Co-morbid conditions such as severe cardiac and/or pulmonary disease
  • Inability to give informed consent

Sites / Locations

  • Asian Institute Of Gastroenterology

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Combination MSC and HSC

Standard of care for Cirrhosis management

Arm Description

Patient will receive a combination of mesenchymal and Hematopoetic stem cell through hepatic artery under fluroscopic guidance

Diuretics, Hepatoprotective agents and Lactulose

Outcomes

Primary Outcome Measures

To assess the safety of combination of hematopoetic and mesenchymal stem cell in patients of liver cirrhosis.
Any adverse events after the use of combination stem cell treatment would be recorded: Bone marrow aspiration related complications such as pain (>6 on VAS) and bleeding from the site. Leukapheresis related complications such as hypotension and hypocalcemia. Hepatic artery catheterization related complications such as pain or discomfort at the catheter insertion site, bleeding and infection. Post MSC and CD34 infusion related adverse reactions would be recorded using CDSCO form.

Secondary Outcome Measures

Change in MELD (Model for End stage Liver disease) score.
Difference in MELD score from baseline to follow-up period.
Change in Child Pugh score.
Difference in Child Pugh score from baseline to follow-up period.
Change in the percentage of CD 34 cells in liver.
To assess improvement in the percentage of CD 34 cells in liver by performing a paired liver biopsy- before and after infusion.

Full Information

First Posted
August 14, 2019
Last Updated
October 20, 2020
Sponsor
Asian Institute of Gastroenterology, India
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1. Study Identification

Unique Protocol Identification Number
NCT04243681
Brief Title
Combination of Autologous MSC and HSC Infusion in Patients With Decompensated Cirrhosis
Official Title
Combination of Autologous Mesenchymal and Hematopoietic Stem Cell Infusion in Patients With Decompensated Cirrhosis: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
July 1, 2019 (Actual)
Primary Completion Date
August 1, 2020 (Actual)
Study Completion Date
September 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Asian Institute of Gastroenterology, India

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Though the results of autologous CD34+ cell infusion and MSC in independent studies have shown promise, yet they are yet to reach the desired long term outcome. The possible postulation for this is possibly because when using autologous CD34+ cell infusion, the inflammatory milieu of the liver may not be conducive for sustained effects of the mobilized CD 34+ cells. MSC have immunomodulatory effect (ref) and may improve the liver environment making it more beneficial for the CD34+ cells to function and survive. In addition, MSC has ben shown to produce hepatocyte growth factor which is protective against liver injury and beneficial for liver regeneration (shown in above tables). However, it remains to be understood how MSCs promote liver stem stem cells to differentiate into hepatocytes or expand the residual hepatocyte population. MSC can also directly inhibit the activation of hepatic stellate cells, the main source of extracellular matrix via MSC derived IL 10 and TNF-αand may also induce hepatic stellate cell apoptosis. Current lacunae in cell based therapy is based on the poor consensus and understanding on the best type of cells to be used, the ideal number of cells, the most appropriate route of administration and the need for repeat dosing . The concept that combination of autologous hematopoietic and mesenchymal stem cells infusion may be more beneficial than infusing any one of them alone has been discussed in many scientific forums but there are no study till date to either see the safety as well as the efficacy of this proof of concept . With this above background data, we propose a study design which will be a safety study for combination use of autologous CD34+ and MSC

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis, Liver
Keywords
Mesenchymal Stem Cell, Hematopoetic Stem cell, Autologous transfusion

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
5 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Combination MSC and HSC
Arm Type
Experimental
Arm Description
Patient will receive a combination of mesenchymal and Hematopoetic stem cell through hepatic artery under fluroscopic guidance
Arm Title
Standard of care for Cirrhosis management
Arm Type
Active Comparator
Arm Description
Diuretics, Hepatoprotective agents and Lactulose
Intervention Type
Combination Product
Intervention Name(s)
CD 34 and MSC infusion
Other Intervention Name(s)
Stem cell infusion
Intervention Description
Combination of stem cells
Intervention Type
Drug
Intervention Name(s)
Standard of care for Cirrhosis management
Intervention Description
Drugs used for Cirrhosis management such as Diuretics, Hepatoprotective agents and Lactulose
Primary Outcome Measure Information:
Title
To assess the safety of combination of hematopoetic and mesenchymal stem cell in patients of liver cirrhosis.
Description
Any adverse events after the use of combination stem cell treatment would be recorded: Bone marrow aspiration related complications such as pain (>6 on VAS) and bleeding from the site. Leukapheresis related complications such as hypotension and hypocalcemia. Hepatic artery catheterization related complications such as pain or discomfort at the catheter insertion site, bleeding and infection. Post MSC and CD34 infusion related adverse reactions would be recorded using CDSCO form.
Time Frame
Up to 6 months
Secondary Outcome Measure Information:
Title
Change in MELD (Model for End stage Liver disease) score.
Description
Difference in MELD score from baseline to follow-up period.
Time Frame
Up to 6 months
Title
Change in Child Pugh score.
Description
Difference in Child Pugh score from baseline to follow-up period.
Time Frame
Up to 6 months
Title
Change in the percentage of CD 34 cells in liver.
Description
To assess improvement in the percentage of CD 34 cells in liver by performing a paired liver biopsy- before and after infusion.
Time Frame
Up to 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 20-70 years Clinically diagnosed for hepatic cirrhosis having a Child Pugh score of B or MELD >10 but below 20 Not willing for immediate liver transplantation either due to lack of donor tissue or financial issues Platelet count of > 80,000 and INR <1.6 Life expectancy of at least 3 months based on MELD score and Child Pugh Score Ability to give informed consent Exclusion Criteria: Age less than 20 or more than 70 years Have liver tumors or history of any other cancer Pregnant or lactating women Patients with hepato-renal syndrome and acute kidney injury (Any creatinine > 1.6 will be excluded) Evidence of ongoing sepsis - as per Surviving sepsis guideline Recent gastrointestinal bleeding or spontaneous bacterial peritonitis (within last one month) Any HIV positive patients Co-morbid conditions such as severe cardiac and/or pulmonary disease Inability to give informed consent
Facility Information:
Facility Name
Asian Institute Of Gastroenterology
City
Hyderabad
State/Province
Telangana
ZIP/Postal Code
500032
Country
India

12. IPD Sharing Statement

Citations:
PubMed Identifier
21900788
Citation
Amer ME, El-Sayed SZ, El-Kheir WA, Gabr H, Gomaa AA, El-Noomani N, Hegazy M. Clinical and laboratory evaluation of patients with end-stage liver cell failure injected with bone marrow-derived hepatocyte-like cells. Eur J Gastroenterol Hepatol. 2011 Oct;23(10):936-41. doi: 10.1097/MEG.0b013e3283488b00.
Results Reference
background
PubMed Identifier
24415865
Citation
Hang HL, Xia Q. Role of BMSCs in liver regeneration and metastasis after hepatectomy. World J Gastroenterol. 2014 Jan 7;20(1):126-32. doi: 10.3748/wjg.v20.i1.126.
Results Reference
background
PubMed Identifier
16556705
Citation
Gordon MY, Levicar N, Pai M, Bachellier P, Dimarakis I, Al-Allaf F, M'Hamdi H, Thalji T, Welsh JP, Marley SB, Davies J, Dazzi F, Marelli-Berg F, Tait P, Playford R, Jiao L, Jensen S, Nicholls JP, Ayav A, Nohandani M, Farzaneh F, Gaken J, Dodge R, Alison M, Apperley JF, Lechler R, Habib NA. Characterization and clinical application of human CD34+ stem/progenitor cell populations mobilized into the blood by granulocyte colony-stimulating factor. Stem Cells. 2006 Jul;24(7):1822-30. doi: 10.1634/stemcells.2005-0629. Epub 2006 Mar 23.
Results Reference
background
PubMed Identifier
35068788
Citation
Sharma M, Pondugala PK, Jaggaihgari S, Mitnala S, Krishna VV, Jaishetwar G, Naik P, Kumar P, Kulkarni A, Gupta R, Singh JR, Darisetty S, Sekharan A, Reddy DN, Rao GV, Syeda F, Jagtap N, Rao PN. Safety Assessment of Autologous Stem Cell Combination Therapy in Patients With Decompensated Liver Cirrhosis: A Pilot Study. J Clin Exp Hepatol. 2022 Jan-Feb;12(1):80-88. doi: 10.1016/j.jceh.2021.03.010. Epub 2021 Apr 2.
Results Reference
derived

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Combination of Autologous MSC and HSC Infusion in Patients With Decompensated Cirrhosis

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