Review of the Registration in the Clinical Research Information Service

Journal of Korean Medical Science
Eun-Kyoung ChoiHyun-Young Park

Abstract

Clinical research registration is required in many countries to improve transparency of clinical research and to ensure subject safety. Developed in February 2010, the Clinical Research Information Service (CRIS) is an online registration system for clinical studies in Korea and one of the primary registries of the World Health Organization (WHO) International Clinical Trials Registry Platform. The present analysis investigated the characteristics of studies registered in the CRIS between February 2010 and December 2014. Data for the analysis were extracted from the CRIS database. As of December 31, 2014, 1,323 clinical studies were registered. Of these, 938 (70.9%) were interventional studies and 385 (29.1%) were observational studies. A total of 248 (18.7%) studies were funded by government sources, 1,051 (79.4%) by non-government sources, and 24 (1.8%) by both. The most frequently studied disease category based on the ICD-10 classification was the digestive system (13.1%), followed by the nervous system (9.4%) and musculoskeletal system (9.1%). Only 17.8% of the studies were registered prior to enrollment of the first subject. Comparing the number of registered or approved clinical studies between the CRIS, the Ministry of F...Continue Reading

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Sep 28, 2017·Journal of Movement Disorders·Timothy E LeeBeomseok Jeon
Apr 10, 2018·Journal of Clinical Neurology·Timothy E LeeBeomseok Jeon
Mar 23, 2017·Revista Panamericana De Salud Pública = Pan American Journal of Public Health·Pablo Rodríguez-Feria, Luis Gabriel Cuervo
Apr 18, 2021·Clinical Trials : Journal of the Society for Clinical Trials·Dilyara NurkhametovaLiliya Eugenevna Ziganshina

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