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Recommendations for the Reporting of Harms in Manuscripts on Clinical Trials Assessing Osteoarthritis Drugs: A Consensus Statement from the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO).

Germain HonvoRaveendhara R BannuruOlivier BruyèreFrancois RannouGabriel Herrero-BeaumontDaniel UebelhartCyrus CooperNigel ArdenPhilip G ConaghanJean-Yves ReginsterThierry ThomasTim McAlindon
Published in: Drugs & aging (2019)
These recommendations may contribute to improve transparency in the field of safety of anti-OA medications. Pharmaceutical companies developing drugs for OA, and researchers conducting clinical trials, are encouraged to comply with them when reporting harms-related results in manuscripts on RCTs. The ESCEO also encourages journals to refer to the ESCEO recommendations in their instructions to authors for the publication of manuscripts on trials of anti-OA medications.
Keyphrases
  • knee osteoarthritis
  • clinical trial
  • clinical practice
  • rheumatoid arthritis
  • adverse drug
  • postmenopausal women
  • phase ii
  • emergency department
  • drug induced
  • open label
  • phase iii
  • double blind
  • electronic health record