The goal of this clinical trial is to learn if Human Umbilical Cord Mesenchymal Stem Cell (HUCMSC) derived secretome injection is safe and effective in patient with liver cirrhosis. The main questions it ams to answer are: 1. How safe is secretome Injection as an adjuvant therapy for liver cirrhosis patients? 2. How effective is secretome injection in liver fibrosis 6 months after injection? 3. Does secretome injection improve liver function after 6 months after Injection? 4. Does secretome injection affect Child Turcotte Pugh score? 5. How does secretome affect pro inflammatory and anti Inflammatory cytokine in patient with liver cirrhosis? 6. How does secretome injection affect the quality of life in live cirrhosis patient? 7. What is the relationship between secretome injection and encephalopathy? Researchers will compare secretome injection group (patients who recieve secretome injections) to best practice treatment group (patient who receive supportive treatment including hepatoprotector and ursodeoxycolic acid) Researchers will compare the intervention group (patients who are injected with HUCMSC derived secretome) and control group (patients who are only monitored and given their usual drugs) Patients will: Be injected with secretome or take hepatoprotector and ursodeoxycolic acid every 2 weeks for 4 months. Do several test such us fibroscan, stroop test, psychometric hepatic encephalopathy score, short form 36 questionnaire, IL-6, TNF alfa and blood test for albumin, SGOT, SGPT, direct bilirubin, indirect bilirubin, INR, creatinine, ureum, hemoglobin, hematocrite, leukocyte, and thrombocyte. Visit the clinic once every two weeks to receive drugs and treatment for 4 months. Follow up visit to review treatment progress on 3rd months (2 weeks post treatment), 7th months (3 months post treatment),10th months (6 months post treatment)
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
54
3 ml Injection of secretome for 8 times two weeks apart
Liver Clinic Prof Ali Sulaiman
Jakarta, DKI Jakarta, Indonesia
Changes in Fibroscan and M2BPGi six month after secretome injections
Patients achieved a response if there are changes in Fibroscan and M2BPGi after secretome injections within six months.best outcome when the M2BPGi Fibroscan decrease, worst outcome when the M2BPGi and Fibroscan increase
Time frame: From enrollment to the end of treatment at 4 months, From enrollment to the end of study at 10 months
Changes in Complete Blood Count and Kidney function after secretome injections
Secretome is safe If hemoglobin and hematocrit, leukocyte, platelet, ureum, and creatinine are still in normal level after secretome injection (best outcome) Secretome is not safe if hemoglobin and hematocrit, leukocyte, platelet, ureum, and creatinine are out of the normal level after secretome injection (worst outcome)
Time frame: From enrollment to the end of treatment at 4 months, From enrollment to the end of study at 10 months
Changes of albumin, SGOT and SGPT levels in six month after secretome injections
Patients achieved a response if there are changes in albumin, SGOT and SGPT levels after secretome injections within six months.best outcome when the albumin, SGOT and SGPT decrease, worst outcome when the albumin, SGOT and SGPT increase
Time frame: From enrollment to the end of treatment at 4 months, From enrollment to the end of study at 10 months
Changes of CTP and MELD score in six month after secretome injections
Patients achieved a response if there are changes in CTP and MELD score after secretome injections within six months.best outcome when the CTP and MELD score decrease, worst outcome when the CTP and MELD score increase
Time frame: From enrollment to the end of treatment at 4 months, From enrollment to the end of study at 10 months
Changes of IL-6 and TNF-α levels in six month after secretome injections
Patients achieved a response if there are changes in IL-6 and TNF-α levels after secretome injections within six months.best outcome when the IL-6 and TNF-α decrease, worst outcome when the IL-6 and TNF-α increase
Time frame: From enrollment to the end of treatment at 4 months, From enrollment to the end of study at 10 months
Changes of Stroop test dan PHES score in six month after secretome injections
Patients achieved a response if there are changes inStroop test dan PHES score after secretome injections within six months.best outcome when the Stroop test dan PHES score increase, worst outcome when the Stroop test dan PHES score decrease
Time frame: From enrollment to the end of treatment at 4 months, From enrollment to the end of study at 10 months
Changes of SF-36 questionnaire score in six month after secretome injections
Patients achieved a response if there are changes in SF-36 questionnaire score after secretome injections within six months.best outcome when the SF-36 questionnaire score increase, worst outcome when the SF-36 questionnaire score decrease
Time frame: From enrollment to the end of treatment at 4 months, From enrollment to the end of study at 10 months
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