TY - JOUR
T1 - Pragmatic clinical trials in CKD
T2 - Opportunities and challenges
AU - American Society of Nephrology Chronic Kidney Disease Advisory Group
AU - de Boer, Ian H.
AU - Kovesdy, Csaba P.
AU - Navaneethan, Sankar D.
AU - Peralta, Carmen A.
AU - Tuot, Delphine S.
AU - Vazquez, Miguel A.
AU - Crews, Deidra C.
N1 - Funding Information:
The San Francisco VA Medical Center and University of California San Francisco CKD screening study is supported by grant R34DK102152 from the National Institute for Diabetes and Digestive and Kidney Diseases (NIDDK). KARE is supported by grants R34DK093992 and R01DK104130 from the NIDDK. ICD-Pieces is supported by grant UH3DK104655 from the NIDDK. The ECHO-CKD study is supported by UH2HL125122 from the National Heart, Lung, and Blood Institute.
Publisher Copyright:
Copyright © 2016 by the American Society of Nephrology.
PY - 2016
Y1 - 2016
N2 - Randomized controlled trials in CKD lag in number behind those of other chronic diseases, despite the high morbidity and mortality experienced by patients with kidney disease and the exorbitant costs of their health care. Observational studies of CKD frequently yield seemingly paradoxic associations of traditional risk factors with outcomes, making it difficult to extrapolate the results of trials conducted in people with normal kidney function to patients with CKD. However, many completed trials in CKD have been limited by intermediate outcomes of unclear clinical significance or narrow eligibility criteria that limit external validity, and implementation of proven therapies remains a challenge. It is therefore imperative that the nephrology community capitalize on recent interest in novel approaches to trial design, such as pragmatic clinical trials. These trials are meant to promote research within real world settings to yield clinically relevant results with greater applicability than those of traditional trials, while maintaining many advantages, such as controlling for potential sources of bias. We provide a description of pragmatic clinical trials and a discussion of advantages, disadvantages, and practical challenges inherent to this study design, in the context of specific scientific questions relevant to patients with CKD.
AB - Randomized controlled trials in CKD lag in number behind those of other chronic diseases, despite the high morbidity and mortality experienced by patients with kidney disease and the exorbitant costs of their health care. Observational studies of CKD frequently yield seemingly paradoxic associations of traditional risk factors with outcomes, making it difficult to extrapolate the results of trials conducted in people with normal kidney function to patients with CKD. However, many completed trials in CKD have been limited by intermediate outcomes of unclear clinical significance or narrow eligibility criteria that limit external validity, and implementation of proven therapies remains a challenge. It is therefore imperative that the nephrology community capitalize on recent interest in novel approaches to trial design, such as pragmatic clinical trials. These trials are meant to promote research within real world settings to yield clinically relevant results with greater applicability than those of traditional trials, while maintaining many advantages, such as controlling for potential sources of bias. We provide a description of pragmatic clinical trials and a discussion of advantages, disadvantages, and practical challenges inherent to this study design, in the context of specific scientific questions relevant to patients with CKD.
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U2 - 10.1681/ASN.2015111264
DO - 10.1681/ASN.2015111264
M3 - Review article
C2 - 27283497
AN - SCOPUS:85019924490
SN - 1046-6673
VL - 27
SP - 2948
EP - 2954
JO - Journal of the American Society of Nephrology
JF - Journal of the American Society of Nephrology
IS - 10
ER -