Adverse event reporting in randomised controlled trials of neuropathic pain: Considerations for future practice

[1]  J. Fox-Rushby,et al.  The Characteristics and Quality of Randomized Controlled Trials in Neuropathic Pain: A Descriptive Study Based on a Systematic Review , 2013, The Clinical journal of pain.

[2]  D. Altman,et al.  The COMET (Core Outcome Measures in Effectiveness Trials) Initiative , 2011, Trials.

[3]  A. Marson,et al.  Reporting of adverse events in randomised controlled trials of antiepileptic drugs using the CONSORT criteria for reporting harms , 2011, Epilepsy Research.

[4]  Su Golder,et al.  Meta-analyses of Adverse Effects Data Derived from Randomised Controlled Trials as Compared to Observational Studies: Methodological Overview , 2011, PLoS medicine.

[5]  H. Kölsch,et al.  Reporting bias in medical research - a narrative review , 2010, Trials.

[6]  J. Anastasi,et al.  Adverse Event Reporting in Acupuncture Clinical Trials Focusing on Pain , 2010, The Clinical journal of pain.

[7]  Isabelle Boutron,et al.  Reporting of safety results in published reports of randomized controlled trials. , 2009, Archives of internal medicine.

[8]  John P A Ioannidis,et al.  Adverse events in randomized trials: neglected, restricted, distorted, and silenced. , 2009, Archives of internal medicine.

[9]  S. Andreassen,et al.  Reporting of adverse events in randomized controlled trials of highly active antiretroviral therapy: systematic review. , 2009, The Journal of antimicrobial chemotherapy.

[10]  P. Dahm,et al.  Reporting of harm in randomized controlled trials published in the urological literature. , 2009, The Journal of urology.

[11]  M. Rowbotham The impact of selective publication on clinical research in pain , 2008, PAIN.

[12]  Robert T. Chen,et al.  The development of standardized case definitions and guidelines for adverse events following immunization. , 2007, Vaccine.

[13]  John P.A. Ioannidis,et al.  Comparison of evidence on harms of medical interventions in randomized and nonrandomized studies , 2006, Canadian Medical Association Journal.

[14]  A. Avins,et al.  Brief Communication: Better Ways To Question Patients about Adverse Medical Events , 2006, Annals of Internal Medicine.

[15]  S. Goodman,et al.  Adverse Events: The More You Search, the More You Find , 2006, Annals of Internal Medicine.

[16]  J. Ioannidis,et al.  Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement , 2004, Annals of Internal Medicine.

[17]  J. Farrar,et al.  Core outcome measures for chronic pain clinical trials: IMMPACT recommendations , 2003, Pain.

[18]  J. Farrar,et al.  Core outcome domains for chronic pain clinical trials: IMMPACT recommendations , 2003, Pain.

[19]  R. Moore,et al.  Reporting of adverse effects in clinical trials should be improved: lessons from acute postoperative pain. , 1999, Journal of pain and symptom management.

[20]  J. Higgins,et al.  Cochrane Handbook for Systematic Reviews of Interventions, Version 5.1.0. The Cochrane Collaboration , 2013 .