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Timing is everything: The importance of patient-reported outcome assessment frequency when characterizing symptomatic adverse events.

Bellinda L King-KallimanisVishal BhatnagarErica G HorodniceanuTing-Yu ChenPaul G Kluetz
Published in: Clinical trials (London, England) (2022)
This analysis demonstrates that more frequent assessment of patient-reported symptomatic adverse events will lead to improved detection, and therefore a more complete understanding of the tolerability of experimental anti-cancer therapies.
Keyphrases
  • patient reported
  • patient reported outcomes
  • open label
  • randomized controlled trial
  • clinical trial
  • label free
  • double blind
  • study protocol
  • placebo controlled