How to report adaptive design randomized trials-A interpretation of international reporting guideline ACE.
10.3760/cma.j.cn112338-20210319-00230
- VernacularTitle:使用适应性设计的随机对照试验报告规范解读
- Author:
Hu Zi Wei ZHOU
1
;
Xue Feng LAI
1
;
Feng SUN
1
;
Munyaradzi DIMAIRO
2
;
Si Yan ZHAN
1
;
Sheng Feng WANG
1
Author Information
1. School of Public Health/Department of Epidemiology and Biostatistics, School of Public Health/Key Laboratory for Research and Evaluation of Pharmacovigilance, National Medical Products Administration/Clinical Epidemiology Research Center, Peking University, Beijing 100191, China.
2. School of Health and Related Research, The University of Sheffield, Sheffield S1 4DP, UK.
- Publication Type:Journal Article
- MeSH:
Checklist;
Humans;
Randomized Controlled Trials as Topic;
Research Design;
Research Report
- From:
Chinese Journal of Epidemiology
2022;43(3):409-417
- CountryChina
- Language:Chinese
-
Abstract:
Concerns has been raised in improving the quality of adaptive design randomized trials reports. Based on the CONSORT 2010 (Consolidated Standards of Reporting Trials), The Adaptive designs CONSORT Extension (ACE) has developed items and reporting specifications for adaptive design trials. This paper presents a brief explanation of the extension and new items of ACE and introduces the applications of ACE checklist with examples.
