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Clinical Trials of SCSNZ Website

CLINICAL TRIALS

Harvesting olfactory mucosa (nasal tissue) that includes both olfactory ensheathing cells (OECs) and stem cells and transplanting them into the injury site within the spinal cord is, at present, the most promising treatment for chronic (long-term) spinal cord injury internationally. The procedure currently performed only in Lisbon, Portugal by Dr Carlos Lima and his team involves carefully opening the spinal cord to reveal the injury site (commonly a fluid filled cavity) and the removal of a small knot of scar tissue present within the injured site.  This prepares the site for transplantation. The olfactory tissue is then removed from the nasal cavity by an Ear, Nose and Throat surgeon, carefully dissected and chopped into very small fragments by Dr Lima. These fragments are then placed into the prepared cavity and the spinal cord closed.

Two web addresses providing further information about Dr Lima's procedure are:

www.healingtherapies.info/OlfactoryTissue1.htm

www.healingtherapies.info/OlfactoryTissue2.htm

So far, Dr Lima and his team have performed this procedure more than 120 times on people from various parts of the world.

An initial report on the first seven Lisbon cases has been published in The Journal of Spinal Cord Medicine in 2006 and provides important information on the relative safety of the surgery. The report indicated that the surgical procedure had no adverse effects. Anecdotal information and personal testimonials have indicated that some patients have regained some sensation and function.

SCSNZ have started planning for an initial Clinical Study for transplantation of autologous olfactory mucosal tissue followed by active rehabilitation therapy as a treatment for spinal cord injury, to be performed in New Zealand. The goal of the initial SCSNZ study will be to demonstrate that the treatment is safe in a NZ environment and evaluate whether or not cell transplantation followed by intensive rehabilitation is better than intensive rehabilitation alone.

Funding for this part of the process is now urgently sought. Ethical approval is required before recruitment and pre-surgical assessments can be made.

Further clinical research studies will be carried out following this initial study. These will involve a type of stem cell from the person's bone marrow and purified olfactory cells grown in the laboratory. See the sections on Adult Stem Cells and Combination Therapy for further information.

 




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