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Trial record 48 of 1807 for:    "bone marrow" | Recruiting, Not yet recruiting Studies

Clinical Trial for Evaluation of Treatment With Multiple Infusions of Mononuclear Bone Marrow Cells in Patients With Chronic Liver Diseases

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT02171949
Recruitment Status : Recruiting
First Posted : June 24, 2014
Last Update Posted : November 28, 2017
Ministry of Science and Technology, Brazil
Ministry of Health, Brazil
Information provided by (Responsible Party):
Ricardo Ribeiro dos Santos, Hospital Sao Rafael

Brief Summary:
The purpose of this study is to evaluate the safety and efficacy of multiple infusions of mononuclear bone marrow cells in patients with chronic liver diseases.

Condition or disease Intervention/treatment Phase
Chronic Hepatitis Hepatic Cirrhosis Biological: Infusion of bone marrow mononuclear cells. Phase 2

Detailed Description:

This is a safety/efficacy phase II, open, randomized, controlled clinical trial, with two arms. The study population will consist of 30 patients with chronic decompensated liver disease (Child-Pugh B or C). The candidates included in the study will be asked to voluntarily participate and sign the written consent.

The patients will be allocated randomly into 2 groups: in group A, the patients will undergo the intervention; and in group B, the patients will be the controls. Patients of both groups will receive clinical follow-up. They will be maintained on drug therapy commonly used in patients with cirrhosis, which may include: spironolactone, furosemide, lactulose, metronidazole, neomycin, analogs of nucleoside / nucleotide in patients with hepatitis B, and vitamin complexes.

All patients included in Group A will undergo cell therapy according to the technique described as follows: on day 1 (D-1), patients will be hospitalized to undergo the bone marrow puncture through the iliac crest. 150 to 200 ml of bone marrow aspirate will be collected. The procedure will be done under local anesthesia and sedation. The fraction of mononuclear cells will be isolated from the aspirated marrow by the SEPAX (System of cell processing) - Biosafe, Switzerland.

The enriched fraction of collected mononuclear cells will be resuspended in saline. The obtained cell populations will be analyzed by flow cytometry for its characterization, and then diluted in 20 ml saline. The cells will be injected 3 times throughout the study, on days 1 (D-1), 30 (D-30) and 60 (D-60).

Patients will undergo a series of clinical and laboratory evaluations and will also be submitted to the following procedures:

  • Cell blood count
  • Biochemical analysis (measurement of electrolytes - sodium and potassium)
  • Renal function tests (urea and creatinine)
  • Liver profile tests (total proteins and fractions, bilirubin, prothrombin time, transaminases, alkaline phosphatase, gamma-GT)
  • Metabolic profile (glucose, total cholesterol and fractions, triglycerides)
  • Thyroid profile tests
  • Serology required for blood transfusion and bone marrow transplant in Brazil
  • Alpha-fetoprotein
  • Beta-HCG (human chorionic gonadotropin), for women
  • Handgrip dynamometer
  • Treadmill test
  • Six-minute walk test
  • Abdomen doppler ultrasound
  • Magnetic resonance imaging of the upper abdomen with elastography
  • Measurement of serum factors
  • Shear wave elastography

Also, the patients will respond to questions from the SF (Short Form) -36 questionnaire (for assessment of quality of life).

Clinical follow-up will be kept for patients who suspend their participation in the study for any adverse event and / or laboratory abnormality, or for the patient's own desire, following insurance protocols. In addition to the clinical and surgical follow-up, specific medical care will be offered to patients who experience adverse events, until stabilization of the patient, even if the target date for completion of the study has been exceeded.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 30 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Treatment
Official Title: Randomized, Open and Controlled Clinical Trial for Evaluation of Treatment With Multiple Infusions of Mononuclear Bone Marrow Cells in Patients With Chronic Liver Diseases
Actual Study Start Date : April 2015
Estimated Primary Completion Date : December 2018
Estimated Study Completion Date : June 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Liver Diseases

Arm Intervention/treatment
No Intervention: Control group
Active Comparator: Bone marrow mononuclear cell therapy Biological: Infusion of bone marrow mononuclear cells.
Patients on this group will receive therapy with mononuclear cells. The cells will be diluted on saline and then injected on the hepatic artery through femoral artery puncture.

Primary Outcome Measures :
  1. Evaluation of Child-Pugh score [ Time Frame: 12 months ]
    Functional class improvement of 2 points on Child-Pugh score.

  2. Evaluation of MELD score [ Time Frame: 12 months ]
    Functional class improvement of 2 points on MELD score.

Secondary Outcome Measures :
  1. Degree of muscle strength [ Time Frame: 12 months ]
    Improvement in the degree of muscle strength assessed using handgrip dynamometer.

  2. Hepatic fibrosis [ Time Frame: 12 months ]
    Decrease of hepatic fibrosis detected by elastography shear waves.

  3. Quality of life [ Time Frame: 12 months ]
    Improvement on the SF-36 questionnaire score, which evaluates quality of life.

  4. Evaluation of functional capacity [ Time Frame: 12 months ]
    Improvement in the functional capacity, assessed by six-minute walk test.

  5. Evaluation of serum bilirubin levels [ Time Frame: 12 months ]
    Improvement in the serum bilirubin levels.

  6. Evaluation of serum albumin levels [ Time Frame: 12 months ]
    Improvement in the serum albumin levels.

  7. Evaluation of prothrombin time [ Time Frame: 12 months ]
    Improvement in prothrombin time.

  8. Evaluation of serum levels of cytokines [ Time Frame: 12 months ]
    Decrease in the serum levels of cytokines.

  9. Evaluation of fibrosis markers levels [ Time Frame: 12 months ]
    Decrease in the serum levels of fibrosis markers.

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Diagnosis of liver cirrhosis of different etiologies, confirmed by clinical examination, laboratory tests, imaging studies and / or biopsy that shows process of evolution to cirrhosis or established cirrhosis (equivalent to Metavir score F3/F4);
  • Non-participation on the waiting list for liver transplantation or, in case of participation, allocation after the fifth position in the list, for subjects with blood group A or O, and after the third position for subjects with other blood groups;
  • Absence of clinical, laboratory and radiological evidence of hepatocellular carcinoma;
  • Absence of pregnancy potential or negative pregnancy test for female patients, or impossibility to use a contraception method during the study;
  • Permission for doing the puncture of iliac crest after evaluation of pre-anesthetic visit.

Exclusion Criteria:

  • Impossibility to obtain vascular access for percutaneous procedure;
  • Sepsis;
  • Hepatic encephalopathy detected at the screening tests;
  • Budd-Chiari syndrome;
  • Severe coagulopathy with INR > 2,4 or platelet count < 30.000;
  • Presence of malignancies (excluding non-melanoma skin cancer);
  • Decompensated heart failure;
  • Primary hematologic diseases;
  • Renal failure with creatinin > 2,5mg/dl;
  • Coinfection with HIV;
  • Pregnancy;
  • Dependence of organic medium such as circulatory or ventilatory;
  • Any other comorbidity with an impact on the survival in 2 years;
  • Participation in other clinical trial.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT02171949

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Contact: André C Lyra, PhD 557132816455

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Hospital São Rafael Recruiting
Salvador, Bahia, Brazil, 41253-190
Contact: André C Lyra, PhD    55713281-6455   
Sponsors and Collaborators
Hospital Sao Rafael
Ministry of Science and Technology, Brazil
Ministry of Health, Brazil
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Principal Investigator: André C Lyra, PhD Hospital São Rafael
Study Chair: Bruno SF Souza, MD, Msc Hospital São Rafael
Study Chair: Eduardo L Braga, PhD Hospital São Rafael
Study Chair: Lourianne N Cavalcante, PhD Hospital São Rafael
Study Chair: Milena BP Soares, PhD Hospital São Rafael
Principal Investigator: Ricardo R dos Santos, PhD Hospital São Rafael
Study Chair: Ticiana F Larocca, MD, Msc Hospital São Rafael

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Responsible Party: Ricardo Ribeiro dos Santos, PhD, Hospital Sao Rafael Identifier: NCT02171949     History of Changes
Other Study ID Numbers: PCL 03/13
First Posted: June 24, 2014    Key Record Dates
Last Update Posted: November 28, 2017
Last Verified: November 2017

Keywords provided by Ricardo Ribeiro dos Santos, Hospital Sao Rafael:
Chronic hepatitis
Hepatic cirrhosis

Additional relevant MeSH terms:
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Hepatitis, Chronic
Liver Diseases
Liver Cirrhosis
Digestive System Diseases
Pathologic Processes