Innovative strategies for trial design

被引:0
|
作者
Feldman, BM
机构
[1] Hosp Sick Children, Div Rheumatol, Dept Paediat, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Dept Paediat, Toronto, ON M5S 1A1, Canada
[3] Univ Toronto, Dept Publ Hlth Sci, Toronto, ON M5S 1A1, Canada
[4] Bloorview MacMillan Ctr, Musculoskeletal Program, Toronto, ON, Canada
关键词
clinical trials; pediatric rheumatology; juvenile rheumatoid arthritis;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Most clinical trial designs used in evaluating therapies require large numbers of subjects. Childhood rheumatic diseases are rare and large numbers of subjects are not available, We have largely been unsuccessful in developing evidence based therapeutics for pediatric rheumatology. Because these diseases are rare, it is important for each clinical trial to enrol all possible subjects, and it is important to extract as much information as possible from each subject. Placebo controlled randomized studies are sometimes seen as unacceptable to physicians and patients. We need study designs that are more acceptable and that will increase accrual. Some clinical trial designs, especially those that involve crossover treatment assignments, can increase the amount of information that each subject contributes. These types of studies can only be used for treatments that are reversible. For treatments that may permanently affect the disease course, I propose the randomized placebo phase design as one way of increasing study acceptability and accrual.
引用
收藏
页码:4 / 7
页数:4
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