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Clinical Trial Summary

This study aims to extract data from the Hong Kong Biologics Registry for retention rate of the JAK inhibitors in rheumatoid arthritis and review other adverse events by looking at the medical record retrospectively. These real life data are important as they cannot be provided by randomized controlled trials which are limited by the duration of observation and fixed protocols in research settings. Moreover, data will represent our local experience of the JAK inhibitors in Chinese patients with RA.


Clinical Trial Description

This study aims to extract data from the Hong Kong Biologics Registry for retention rate of the JAK inhibitors in rheumatoid arthritis and review other adverse events by looking at the medical record retrospectively. Efficacy data and adverse events, in particular major adverse cardiovascular events (MACEs) and malignancy will be looked at and compared with the TNF inhibitors. Retention / withdrawal rates of the drugs will be studied by statistical analyses. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05182203
Study type Observational [Patient Registry]
Source Tuen Mun Hospital
Contact Chi Chiu Mok, MD, FRCP
Phone 852-37677844
Email [email protected]
Status Not yet recruiting
Phase
Start date January 2022
Completion date December 2022

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