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Clinical Trials/NCT01504594
NCT01504594
Suspended
Phase 1

Safeness and Effectiveness of Autologous Hematopoietic Cell Infusion Through Catheterization in Pediatric Patients With Dilated Cardiomyopathy

Hospital Universitario Dr. Jose E. Gonzalez1 site in 1 country10 target enrollmentJanuary 2012

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Cardiomyopathy, Dilated
Sponsor
Hospital Universitario Dr. Jose E. Gonzalez
Enrollment
10
Locations
1
Primary Endpoint
Safeness of autologous bone marrow derived stem cells infused through cardiac catheterization to coronary arteries.
Status
Suspended
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this study is to determine whether an autologous stem cell infusion through catheterism is safe and effective in the treatment of pediatric dilated cardiomyopathy.

Process:

  1. Primary Evaluation

    • Clinical History
    • Echocardiogram to evaluate ejection fraction and other parameters
  2. Signing of Informed Consent and clearing doubts

  3. Bone Marrow stimulation for 3 consecutive days with G-CSF (Granulocyte Colony Stimulating Factor) applied subcutaneously

  4. On the 4th day, in operation room and under sedation: Bone Marrow Harvest performed by hematologists through posterior iliac crests(amount calculated at 8cc/kg, without exceeding 150ml).

  5. Recovery room with family members while the cells are being processed in the Hematology Laboratory.

  6. Approximately 3 hours after the 1st procedure, the patient re-enters the operation room, which is equipped for cardiac catheterization, so that cardiologists infuse the stem cells through the femoral artery into the coronary arteries which irrigate the heart´s muscle fibers.

  7. Patient goes back to the recovery area until the anesthesia effect is gone and can tolerate oral liquids.

  8. Clinical and echocardiographic follow-ups at 6 weeks and 6 months after the procedure.

Detailed Description

* The Patient will receive standard surgical care, accompanied by a nurse at all times. * Premedication includes: Omeprazole (gastric protector), Ketorolac (anti-pain and swelling), ondansetron (antivomiting).

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
August 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Hospital Universitario Dr. Jose E. Gonzalez
Responsible Party
Principal Investigator
Principal Investigator

Consuelo Mancias Guerra

Pediatric Hematology Professor

Hospital Universitario Dr. Jose E. Gonzalez

Eligibility Criteria

Inclusion Criteria

  • Ejection fraction less than 35 percent in echocardiogram
  • More than 3 months with complete medical treatment without significant improvement
  • Complete medical treatment: digitalics, diuretics, vasodilators and beta blockers

Exclusion Criteria

  • Not signing informed consent
  • Active infection at enrolling time
  • Inadequate G-CSF application

Outcomes

Primary Outcomes

Safeness of autologous bone marrow derived stem cells infused through cardiac catheterization to coronary arteries.

Time Frame: 6 weeks

Patient will be assessed to prove that the procedure did not cause any deterioration of his/her health presented at the beginning of the study.

Secondary Outcomes

  • Effectiveness of autologous bone marrow derived stem cells infused through cardiac catheterization to coronary arteries.(6 months)

Study Sites (1)

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