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Investigating the effect of mesenchymal stem cell injection on reducing complications in patients with liver cirrhosis

Investigating the effect of intravenous injection of deciduous tooth pulp mesenchymal stem cells in patients with uncompensated liver cirrhosis in order to reduce the complications of the disease

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140911019125N11
Enrollment
10
Registered
2024-08-05
Start date
2024-08-22
Completion date
Unknown
Last updated
2024-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Reducing complications of liver failure in patients with decompensated liver cirrhosis. Congenital cirrhosis (of liver)

Interventions

Intervention 1: Intervention group: In the intervention group, after selecting the patients, a sample of mesenchymal stem cells is injected intravenously at the rate of 1 million per kilogram of body

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Having clinical and laboratory manifestations related to uncompensated liver cirrhosis Age between 18 and 65 years Absence of pregnancy in women There is no specific treatment for cirrhosis Consent to participate in the study

Exclusion criteria

Exclusion criteria: Having an underlying malignancy Evidence of extrahepatic biliary diseases Active thrombosis in the hepatic or portal vein Respiratory or kidney failure Active infection Liver transplantion candidate patients Patients with diabetes mellitus Patients with severe cardiovascular disease and high blood pressure not controlled by medication The presence of severe underlying diseases pregnant women

Design outcomes

Primary

MeasureTime frame
Check liver function. Timepoint: At intervals of 3 and 6 months after injection. Method of measurement: Examining the laboratory parameters of the patient related to the liver with a laboratory device.;Evaluation of the Child-pugh criterion. Timepoint: 3 and 6 months after injection. Method of measurement: Completing certain questionnaires according to laboratory and clinical results of patients.;Evaluation of the MELD criterion. Timepoint: 3 and 6 months after injection. Method of measurement: Completing certain questionnaires according to laboratory and clinical results of patients.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Farsinejad

Kerman University of Medical Sciences

afarsinejad@kmu.ac.ir+98 34 3132 5374

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026