Please post any CCSVI Clinical Trial Information

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.

Postby magoo » Wed Dec 09, 2009 5:58 pm

Only that the info gained by doing the surgery on us has enabled Dr. Dake to properly set up the clinical trial. He seemed very positive about it.
I did not get any info on how they were funding it. It didn't seem to be an issue. He just said it was the next logical step.
It seemed he was disappointed to have to stop the surgeries. The whole thing has become complicated and although he understands, he's not happy about the opposition he's encountering with the Neurology Dept.
Treated by Dake 10/19/09, McGuckin 4/25/11 and 3/9/12- blockages in both IJVs, azy, L-iliac, L-renal veins. CCSVI changed my life and disease.
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Postby Mikkysgl » Thu Dec 10, 2009 1:40 pm

how does one get a hold of dake's office? while he has stopped surgeries i wonder if he is still testing? my nuero indicated that stanford would be a place for trials on this procedure, so not all nueros are roadblocking, of course he is a non- believer until there are massive studies etc.
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