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Patients will be screened and randomized from January 2009 until June 2011.
Two hundred and one elderly participants with very mild to mild dementia will be screened and randomized into the following groups: (i) dance movement based intervention, (ii) stretching and exercise intervention and (iii) no intervention waitlist-control group.
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Overall, 133 patients were screened and randomized to active treatment.
A total of 148 patients with a current history of migraine were screened and randomized to the two study groups.
A total of 160 patients were screened and randomized into the study between 1 January 2006 and 30 June 2007.
Based on a power calculation for analysis of transfusion requirements, 60 subjects were planned; 80 patients were screened and randomized to the fibrinogen concentrate or placebo groups.
Subjects (n = 95) were screened and randomized to receive glucosamine sulfate (n = 47, 1500 mg/day) or reparagen (n = 48, 1800 mg/day), a polyherbal consisting of 300 mg of vincaria (Uncaria guianensis) and 1500 mg of RNI 249 (Lepidium meyenii) administered orally, twice daily.
To detect a 10-mmHg difference in systolic blood pressure between the randomized groups with the standard deviation set at 20 mmHg and a two-sided p-value of 0.01 and 90% power, 480 patients would have to be screened and 240 randomized, assuming 50% screening failures.
Approximately 1400 patients will be screened and 350 patients will be randomized in <2 years.
A total of 95 patients were screened, and 84 were randomized into the following groups: placebo (n = 28); BTX-A 25U (n = 27); BTX-A 75U (n = 29).
To determine if LA is able to stimulate cAMP production in vivo in human subjects with multiple sclerosis, thirty-six subjects were screened and 29 were randomized to receive 1 of 3 formulations of LA: A, B or C. The formulations differ in composition and were obtained from different companies (see materials and methods).
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