Singapore Clinical Survey Report on Urah TGC (July 2009)
Number of Clinics & Physicians: 16
Number of patients: 44 (Male 22, Female 22)
Duration: 4 weeks average
Summary of Report: Among44 patients who receivedUrahTransdermal GlucosamineCream (Containing 8% Glucosamine Sulphate), the mean Visual Analog Scale scores for pain decreased by34% within the average period of 4 weeks; and no single side effect was recorded.
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Open trial of URAH TRANSDERMALGLUCOSAMINE CREAM in the treatment of pain in Osteoarthritis Patients
(1st Phase Report Released on the 9th April 2008)
By, Prof. O. O. Adelowo (Consultant Rheumatologist) & Dr. s. Oguntona (Consultant Physician), Olabisi Onabanjo University Teaching Hospital, Sagamu.
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A randomized, double blind, Placebo controlled trial of a topical cream containing glucosamine sulfate, chondroitin sulfate, and camphor for osteoarthritis of the Knee
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URAH Transdermal at WHAT Medicine Conference & Exhibition 19th-21st June 2009, Kuala Lumpur, Malaysia.
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Initial results of National Institutes of Health (NIH) Funded Study Reveal Oral Glucosamine and Chrondroitin Not Effective in Treating Moderate to Serve Osteoarthritis knee pain
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J Pharm Pharmaceut Sci (www.ualberta.ca/~csps) 5(2): 181-184, 2002
Single Dose Pharmacokinetics and bioavailability of Glucosamine in the RAT
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Br J Sports Med c 2003; 37;45-49 2003 BMJ Publishing Group & British Association of Sport and Exercise Medicine
The effect of glucosamine supplementation on people experiencing regular Knee pain
R Braham1, B Dawson1 and C Goodman1
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Placebo-Controlled trials
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Arzneimittelforschung. 1993 Oct;43 (10): 1109-13
Pharmacokinetics of glucosamine in main
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