Statistical considerations in reporting cardiovascular research

Statistical and methodological considerations for reporting RCTs in medical literature

Randomized controlled trials (RCTs) are known to provide the most reliable evidence on intervention. However, RCTs are often conducted and reported incompletely and inadequately, making readers and reviewers unable to judge the validity and reliability of the trials. In this article, we consider the statistical and methodological issues involved in reporting on RCTs, particularly in relation to...

The FDA's Final Rule on Expedited Safety Reporting: Statistical Considerations

In March 2011, a Final Rule for expedited reporting of serious adverse events took effect in the United States for studies conducted under an Investigational New Drug (IND) application. In December 2012, the U.S. Food and Drug Administration (FDA) promulgated a final Guidance describing the operationalization of this Final Rule. The Rule and Guidance clarified that a clinical trial sponsor shou...

Standards for Reporting Qualitative Research

سخن سردبیر Editorial مجله دانشگاه علوم پزشکی رفسنجان دوره هجدهم، آذر 1398، 860-859       استاندارد‌هایی برای گزارش پژوهش‌‌های کیفی Standards for Reporting Qualitative Research     محسن رضائیان[1]   M. Rezaeian   تاکنون در مجله علمی دانشگاه، مقالات گوناگونی در خصوص استاندارد‌های تدوین شده برای گزارش شفاف پژوهش‌های کمّی و از جمله کارآزمایی‌‌های بالینی [1] و مطالعات مشاهده‌ای اپیدمیو...

Guidelines on Statistical Reporting at Nicotine & Tobacco Research

permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. Despite the broad array of tools available, we in the biomedical sciences have become limited in the way we do statistical inference, with null hypothesis significance testing (NHST) the dominant approach and small P values the measure of our worth. However, there are a number...

Letter to the Editor: Appropriate Statistical Analysis and Research Reporting