원문정보
초록
영어
In clinical trials, it is important to have well designed case report forms (CRF) in order to obtain good quality of data. If CRF design at the first stage of your study goes wrong, after all efforts have been made, you may find practical difficulties in data analysis at the final stage of your study because of incomplete or wrong information. In this paper, the following rules fundamental to CRF design are introduced: rules in general, rules of format or style, categorized responses, forms with multiple records per subject, and international studies. Investigators are well aware of research goals, however sometimes they do not know how to express it on CRF. If they understand the rules fundamental to CRF design, time for CRF development will be saved and CRF completeness will be enhanced.
목차
일반적 원칙
양식에 관학 원칙
범주형 자료 기록에 관한 원칙
피험자당 다수의 레코드를 허용하는 양식에 관한 원칙
다국가/다기관 임상시험에 필요한 원칙
결 론
감사의 말씀
참고문헌
