Status:

UNKNOWN

Potential Use of Autologous and Allogeneic Mesenchymal Stem Cells in Patients With Multiple System Atrophy

Lead Sponsor:

Indonesia University

Conditions:

Multiple System Atrophy

Parkinsonism

Eligibility:

All Genders

Phase:

NA

Brief Summary

The prevalence of Multiple System Atrophy (MSA) is reported to be between 3.4 - 4.9 cases per 100,000 population. The estimated average incidence is 0.6 - 0.7 cases per 100,000 people per year. Many p...

Eligibility Criteria

Inclusion

  • Patients developed MSA based on clinical examination and consensus MSA criteria.
  • Patients diagnosed with MSA for less than 4 years.
  • Patients with an anticipated survival of at least 3 years in the opinion of the examiner.
  • Patients with MOCa and Mini Mental State Examination (MMSE) values of more than 24.
  • For Adipose Autologous-MSC group subjects were not experiencing active infection, which was confirmed by screening for HbSAg, Anti HCV, Syphilis, HIV, CMV, Rubella, and Toxoplasma.
  • Subjects are willing to participate in research and fill out an informed consent form.
  • Do not have autoimmune disorder, or undergoes management disorders and / or other diseases related to MSA
  • Subjects are willing to participate in research and fill out an informed consent form.

Exclusion

  • Suffer from systemic autoimmune diseases (systemetic lupus erythomatosus, Addison's disease, Crohn's disease, arthritis management), immunodeficiency (SIDA), or blood clotting disorders or management of malignant diseases (diseases associated with MSA)
  • Undergo immunosuppressive therapy, anticoagulants or corticosteroids.
  • Patients with malignant neoplasms and close family history of neoplasms.
  • already had history of spinal surgery, have paralysis or have spinal diseases.
  • Patients with a history of electroconvulsive therapy.
  • Patients with a history of brain surgery for Parkinson's disease.
  • Patients with systemic or local infections located close to the injection site.
  • Undergo immunosuppressive therapy, anticoagulants or corticosteroids.
  • The patient was not willing to take part in the study and did not fill out informed consent.

Key Trial Info

Start Date :

October 5 2020

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 5 2021

Estimated Enrollment :

15 Patients enrolled

Trial Details

Trial ID

NCT04876326

Start Date

October 5 2020

End Date

October 5 2021

Last Update

May 6 2021

Active Locations (1)

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1

Cipto Mangunkusumo General Hospital

Jakarta Pusat, DKI Jakarta, Indonesia