Safety and Feasibility of Human Umbilical Cord Mesenchymal Stem Cell-Derived Secretome in the Treatment of Liver Cirrhosis: a Comprehensive Evaluation of Fibrosis Reduction, Immunomodulation, and Hepatic Regeneration: a Single Center, Randomized, Phase I Clinical Trial

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age17+
SponsorBaermed

About this trial

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)

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age above 17 years, both men and women

Patient is willing to participate and sign informed consent

Patient is diagnosed with liver cirrhosis confirmed by clinical examination and diagnostic imaging

Liver cirrhosis patient with Child-Pugh Class B

Disqualifiers

Patient with uncontrolled psychiatric disorders

Patient who is diagnosed with hepatic or non- hepatic malignancy

Lactating and pregnant patient

Patient who has allergy or hypersensitivity reaction towards secretome

Trial design

Design model

Parallel

Treatments tested in this trial

  • Secretome

    Drug

    3 ml Injection of secretome for 8 times two weeks apart

Treatment groups

54 Participants
are divided into 2 treatment groups
Group A: Secretome InjectionExperimental treatment 1 intervention
Group B: Best Treatment PracticeNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

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
2

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
3

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

Secondary outcomes

1

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
2

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
3

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
4

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

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Baermed

Lead sponsor

Tarumanagara University

Collaborator

Liver Clinic Prof Ali Sulaiman

Collaborator

Pelni Hospital

Collaborator

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