4.7 Article

Challenges in conducting clinical trials in nephrology: conclusions from a Kidney Disease-Improving Global Outcomes (KDIGO) Controversies Conference

期刊

KIDNEY INTERNATIONAL
卷 92, 期 2, 页码 297-305

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.kint.2017.04.019

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资金

  1. KDIGO
  2. Abbvie
  3. Achillion
  4. Akebia Therapeutics
  5. Alexion
  6. Amgen
  7. AstraZeneca
  8. Bayer HealthCare
  9. Fresenius Medical Care
  10. KBP Biosciences
  11. Keryx Biopharmaceuticals
  12. Merck
  13. Omeros
  14. Relypsa
  15. Roche
  16. Vifor Fresenius Medical Care Renal Pharma
  17. Medical Research Council [MC_U137686853, MC_UU_12026/5, MC_UU_12026/4, MC_UU_12026/6] Funding Source: researchfish
  18. Steno Diabetes Center Copenhagen (SDCC) [SDCC 3.A Complications] Funding Source: researchfish
  19. MRC [MC_U137686853, MC_UU_12026/4, MC_UU_12026/5, MC_UU_12026/6] Funding Source: UKRI

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Despite the high costs of treatment of people with kidney disease and associated comorbid conditions, the amount of reliable information available to guide the care of such patients is very limited. Some treatments have been assessed in randomized trials, but most such trials have been too small to detect treatment effects of a magnitude that would be realistic to achieve with a single intervention. Therefore, KDIGO convened an international, multidisciplinary controversies conference titled Challenges in the Conduct of Clinical Trials in Nephrology to identify the key barriers to conducting trials in patients with kidney disease. The conference began with plenary talks focusing on the key areas of discussion that included appropriate trial design (covering identification and evaluation of kidney and nonkidney disease outcomes) and sensible trial execution (with particular emphasis on streamlining both design and conduct). Break out group discussions followed in which the key areas of agreement and remaining controversy were identified. Here we summarize the main findings from the conference and set out a range of potential solutions. If followed, these solutions could ensure future trials among people with kidney disease are sufficiently robust to provide reliable answers and are not constrained by inappropriate complexities in design or conduct.

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