Clinical trials are a fundamental component of medical research and serve as the main route to obtain evidence of the safety and efficacy of treatment before its approval. A trial's ability to provide the intended evidence hinges on appropriate design, background knowledge, trial rationale to sample size, and interim monitoring rules. In this article, we present some general design principles for investigators and their research teams to consider when planning to conduct a trial.
|Original language||English (US)|
|Number of pages||4|
|Journal||Journal of Thoracic Oncology|
|State||Published - Aug 2020|
- Clinical trial
ASJC Scopus subject areas
- Pulmonary and Respiratory Medicine