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Woo: Clinical Outcome Research through Patient Registries
Statement

J Korean Diabetes 2015;16(3):168-173.

Published online: 10 January 2015

DOI: https://doi.org/10.4093/jkd.2015.16.3.168

Clinical Outcome Research through Patient Registries

Jeong-Taek Woo

Department of Endocrinology and Metabolism, Kyung Hee University School of Medicine, Seoul, Korea

Corresponding author: Jeong-Taek Woo Department of Endocrinology and Metabolism, Kyung Hee University Hospital, 23 Kyungheedae-ro, Dongdaemun-gu, Seoul 02774, Korea, E-mail: jtwoomd@khmc.or.kr

Received 14 August 2015       Accepted 18 August 2015

Copyright © 2015 Korean Diabetes Association

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

As our population ages, so grows the amount of medical expenditures. In the future, elderly people will be better organized, more assertive and have higher expectations of their quality of life. More advanced health technologies have been developed with potential harm as well as beneficial effectiveness. We should provide the patients with health technologies with high scientific evidences. Randomized control trials (RCTs) provide the highest level of scientific evidence, but cannot always be performed because of ethical, practical or financial limitations, and do not always reflect what occurs in real clinical practice. However, patient registries can be used to evaluate patient outcomes through prospective evaluation of a structured collection of clinical information. Therefore, patient registries can complement RCTs.

Keywords: Clinical outcome, Clinical research, Patient registry

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