Status:

WITHDRAWN

Study to Assess the Safety and Effects of Autologous Adipose-Derived Stromal Cells in Patients After Stroke

Lead Sponsor:

Ageless Regenerative Institute

Collaborating Sponsors:

Instituto de Medicina Regenerativa

Conditions:

Stroke

Eligibility:

All Genders

18-80 years

Phase:

PHASE1

PHASE2

Brief Summary

The intent of this clinical study is to answer the questions: 1. Is the proposed treatment safe 2. Is treatment effective in improving the disease pathology of patients after Stroke and clinical outc...

Detailed Description

Adipose-Derived Stromal Cells (ASCs) are a novel therapy for patients suffering from stroke. By injecting ASCs either into the internal carotid artery, these regions may become populated with the ASCs...

Eligibility Criteria

Inclusion

  • Males and Females between Age 18 and 80 years.
  • Symptoms and signs of clinically definite ischemic stroke or hemorrhagic stroke
  • DWI-MRI has reliably shown relevant ischemic lesions
  • Extracranial duplex/transcranial Doppler must confirm intra/extracranial arteries permeability
  • The stroke is severe (NIH Stroke Scale \>= 8 before procedure)
  • Up to date on all age and gender appropriate cancer screening per American Cancer Society.

Exclusion

  • Females who are pregnant or nursing or females of childbearing potential who are unwilling to maintain contraceptive therapy for the duration of the study
  • Life expectancy \< 6 months due to concomitant illnesses.
  • Exposure to any investigational drug or procedure within 1 month prior to study entry or enrolled in a concurrent study that may confound results of this study.
  • Active infectious disease and/or known to have tested positive for HIV, HTLV, HBV, HCV, CMV (IgM \> IgG) and/or syphilis will have expert consultation to determine eligibility based on the patient's infectious status
  • Any illness which, in the Investigator's judgment, will interfere with the patient's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of the study results
  • Patients on chronic immunosuppressive transplant therapy
  • Systolic blood pressure (supine) ≤90 mmHg or greater than 180mmHg
  • Resting heart rate \> 100 bpm;
  • Active clinical infection being treated by antibiotics within one week of enrollment.
  • Known drug or alcohol dependence or any other factors which will interfere with the study conduct or interpretation of the results or who in the opinion of the investigator are not suitable to participate.
  • History of cancer (other than non-melanoma skin cancer or in-situ cervical cancer) in the last five years.
  • Unwilling and/or not able to give written informed consent.

Key Trial Info

Start Date :

October 1 2014

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2015

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT01453829

Start Date

October 1 2014

End Date

June 1 2015

Last Update

July 21 2017

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Hospital Angeles

Tijuana, Estado de Baja California, Mexico, 22010