Design of clinical trials in acute kidney injury: report from an NIDDK workshop on trial methodology.

Published

Journal Article

Acute kidney injury (AKI) remains a complex clinical problem associated with significant short-term morbidity and mortality and lacking effective pharmacologic interventions. Patients with AKI experience longer-term risks for progressive chronic ESRD, which diminish patients' health-related quality of life and create a larger burden on the healthcare system. Although experimental models have yielded numerous promising agents, translation into clinical practice has been unsuccessful, possibly because of issues in clinical trial design, such as delayed drug administration, masking of therapeutic benefit by adverse events, and inadequate sample size. To address issues of clinical trial design, the National Institute of Diabetes and Digestive and Kidney Diseases sponsored a workshop titled "Clinical Trials in Acute Kidney Injury: Current Opportunities and Barriers" in December 2010. Workshop participants included representatives from academia, industry, and government agencies whose areas of expertise spanned basic science, clinical nephrology, critical care medicine, biostatistics, pharmacology, and drug development. This document summarizes the discussions of collaborative workgroups that addressed issues related to patient selection, study endpoints, the role of novel biomarkers, sample size and power calculations, and adverse events and pilot/feasibility studies in prevention and treatment of AKI. Companion articles outline the discussions of workgroups for model trials related to prevention or treatment of established AKI in different clinical settings, such as in patients with sepsis.

Full Text

Cited Authors

  • Palevsky, PM; Molitoris, BA; Okusa, MD; Levin, A; Waikar, SS; Wald, R; Chertow, GM; Murray, PT; Parikh, CR; Shaw, AD; Go, AS; Faubel, SG; Kellum, JA; Chinchilli, VM; Liu, KD; Cheung, AK; Weisbord, SD; Chawla, LS; Kaufman, JS; Devarajan, P; Toto, RM; Hsu, C-Y; Greene, T; Mehta, RL; Stokes, JB; Thompson, AM; Thompson, BT; Westenfelder, CS; Tumlin, JA; Warnock, DG; Shah, SV; Xie, Y; Duggan, EG; Kimmel, PL; Star, RA

Published Date

  • May 2012

Published In

Volume / Issue

  • 7 / 5

Start / End Page

  • 844 - 850

PubMed ID

  • 22442182

Pubmed Central ID

  • 22442182

Electronic International Standard Serial Number (EISSN)

  • 1555-905X

Digital Object Identifier (DOI)

  • 10.2215/CJN.12791211

Language

  • eng

Conference Location

  • United States