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Indian Stem Cell Trial to Broaden Diabetic Foot Inclusion Criteria
Date:9/16/2009

l now be able to examine the potential of peripheral blood-derived stem cells to induce neovascularization," Lalit continued, "The clinical value of bone marrow stem cells has been known for years, and we hear about fetal and embryonic stem cells in the news every day. In this study, though, we are processing a patient's own blood to isolate stem cells and then using these stem cells to treat their diabetic foot ulcers and circulatory problems. When this trial is over we will have confirmed whether a diabetic patient's own peripheral blood can be used to induce the growth of new blood vessels in their damaged tissue."

The clinical trial is officially titled, "A Randomized, Controlled, Parallel Design, Safety and Efficacy Study of Granulocyte Colony Stimulating Factor Mobilized Autologous Peripheral Blood Mononuclear Cell Therapy in Subjects With Diabetic Limb Ischemia." India's Council of Medical Research approved the study after verifying that it met all associated criteria in terms of design and controls as well as following ethical and safety standards.

"The large number of people who applied to enroll in this study confirms that there is strong demand for this therapy and a need to augment current treatment methods. However, to enroll enough subjects for a successful study we have determined that we must broaden the inclusion criteria and reapply to ICMR. Now that we have notified the ICMR we will restart the trial in October," said Dr. Anoop Misra.

About this Clinical Trial

For more information, please use this trial's ID: NCT00922389 on the U.S. National Institute of Health's Clinical Trial Listings: http://www.clinicaltrials.gov

About Fortis Healthcare, India

Fortis Healthcare Limited ( '/>"/>

SOURCE Shenzhen Beike Biotechnology Co. Ltd.
Copyright©2009 PR Newswire.
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