Alerts
PDF
Other content recommended for you
- Informed consent in cluster randomised trials: a guide for the perplexed
- Ethical issues raised by cluster randomised trials conducted in low-resource settings: identifying gaps in the Ottawa Statement through an analysis of the PURE Malawi trial
- The Ottawa Statement on the ethical design and conduct of cluster randomised trials: précis for researchers and research ethics committees
- Ottawa Statement does not impede randomised evaluation of government health programmes
- Impact of the 2011 ACGME resident duty hour reform on hospital patient experience and processes-of-care
- Research ethics for emerging trial designs: does equipoise need to adapt?
- Informed consent in pragmatic trials: results from a survey of trials published 2014–2019
- Association of residency work hour reform with long term quality and costs of care of US physicians: observational study
- National improvements in resident physician-reported patient safety after limiting first-year resident physicians’ extended duration work shifts: a pooled analysis of prospective cohort studies
- Ethical implications of excessive cluster sizes in cluster randomised trials