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Autologous Bone Marrow Stem Cells in Middle Cerebral Artery Acute Stroke Treatment.

H

Hospital Universitario Central de Asturias

Status and phase

Completed
Phase 2
Phase 1

Conditions

Infarction, Middle Cerebral Artery
Stroke, Acute

Treatments

Procedure: Infusion on autologous CD34+ stem cells into middle cerebral artery

Study type

Interventional

Funder types

Other

Identifiers

NCT00761982
OVISEV-01

Details and patient eligibility

About

The aim of the study is to determine the safety and efficacy on an autologous CD34+ subset bone marrow stem cell infusion into the middle cerebral artery in patients who have suffered acute middle cerebral artery stroke.

Full description

The proposed trial will involve the recruitment of a total of 20 patients.

The cells will be collected from ten subject recruited as cases, via bone marrow sampling. The aspirate will be centrifuged on a Ficoll density gradient to isolate mononuclear cells, which will be resuspended in heparinized isotonic saline for infusion into the area of the stroke intra-arterially using the middle cerebral artery.

The investigators will monitor each case and control for a period of 6 months post-stem cell infusion. Initially, they will be subjected to a review after one month,three months and finally 6 months.

Assessment of adverse events will be by physical examination and measurement of laboratory parameters. Assessment of efficacy will be by physical examination and the measurement of laboratory, CT and MRI parameters.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Symptoms and signs of clinically definite middle cerebral artery acute stroke.
  • Time of stroke onset is known and treatment can be started between day 5 and 9 of onset.
  • DWI-MRI has reliably shown relevant acute ischemic lesions
  • Extracranial duplex/transcranial Doppler must confirm intra/extracranial arteries permeability.
  • The stroke is severe (NIH Stroke Scale >= 8 before procedure).
  • An age range of 18-80 years old.

Exclusion criteria

  • Patients out of inclusion age range.
  • Lacunar infarction.
  • Patients with cancer.
  • Patients with present or previous malignant disease during the last 5 years, except for basal cell carcinoma.
  • Hematological causes of stroke.
  • Severe co-morbidity.
  • Hepatic or renal dysfunction.
  • The patient is female and of childbearing potential (unless it is certain that pregnancy is not possible) or breast feeding.
  • Patient is likely to be unavailable for follow-up.
  • Patient with evidence of life threatening infection of life threatening illness.
  • Patient was already dependent in activities of daily living before the present acute stroke.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 1 patient group

bone marrow stem cells
Other group
Description:
Procedure: Infusion of autologous CD34+ stem cells into middle cerebral artery.
Treatment:
Procedure: Infusion on autologous CD34+ stem cells into middle cerebral artery

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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