Umbilical Cord Mesenchymal Stem Cell for Aging-related Low-grade Inflammation

About this trial

Last updated 2 years ago

Study ID

133/QĐ-BYT

Status

Active not recruiting

Type

Interventional

Phase

Phase 1

Placebo

Accepting

40 to 64 Years

All Sexes

Trial Timing

Started 3 years ago

What is this trial about?

The goal of this single-group, open-label, phase I/II clinical trial is to evaluate the safety and efficacy of the transplantation of umbilical cord mesenchymal stem cells in aging-related low-grade inflammation patients' pro-inflammatory cytokines. The main questions to answer are: * Is the transplantation of umbilical cord mesenchymal stem cells in aging-related low-grade inflammation patients safe? * Comparison of the expression levels of pro-inflammatory cytokines (IL-1α/β, TNF-α/β, IL-6, IL-11, IL-18, IFN-γ) in the patient's blood before (day 0), after 90 days, and after 180 days of cell transplantation. * Comparison of the expression levels of anti-inflammatory cytokines (IL-10, TGFβ, IL-1) in the patient's blood before (day 0), after 90 days, and after 180 days of cell transplantation. * Comparison of the inflammation balance by the ratios of pro-inflammatory cytokines to anti-inflammatory cytokines in the patient's blood before (day 0), after 90 days, and after 180 days of cell transplantation. * Comparison of the HbA1C index in the diabetes patient's blood before (day 0), after 90 days, and after 180 days of cell transplantation. * Comparision of the indices of Cholesterol, Triglyceride, LDLc, HDLc in the dislipidemia patient's blood before (day 0), after 90 days, and after 180 days of cell transplantation. * Comparison of the BMI in the obese patient's blood before (day 0), after 90 days, and after 180 days of cell transplantation. * Determination of adverse effect frequency in the patients before (day 0), during, after 90 days, and after 180 days of cell transplatation. Participants will receive two intravenous infusions of 100 million umbilical cord mesenchymal stem cells on days 0 and 90. The patient will be monitored for safety and measured as per the study protocol until day 180.

What are the participation requirements?

Inclusion Criteria

* Male or female aged 40-64 years

* TNF-α index > 11 pg/ml and IL6 index > 1.23 pg/ml

* Possesion of at least two of the following three comorbidities: diabetes, dyslipidemia, and obesity

* Stable use of medications for the previous 3 months to treat the previously mentioned comorbidities

* Agreement to participate in the study and to comply with the research examination and evaluation process

Exclusion Criteria

* Patients with coagulopathy

* History of or current severe heart failure

* Acute respiratory disease at the time of screening

* Patients with cancer or other acute illness requiring treatment

* History of allergy to anesthetics and antibiotics

* Currently/planning to participate in another clinical trial during the study period

* Possessing additional conditions or circumstances that make it difficult to provide treatment, according to the researcher Pathology of disease in the exclusion criteria was defined according to the Guidelines of the Ministry of Health of Vietnam.