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Clinical Trial Summary

This study includes RA patients in pregnancy, who are using different treatment regimens,including prednisone, hydroxychloroquine, and/or TNF inhibitors. The maternal disease activity, pregnancy outcomes, maternal and fetal safety are assessing during the trimester of pregnancy. The effects of different therapies and risk factors for adverse pregnancy outcomes will be analysis.


Clinical Trial Description

To study the risk factors of poor pregnancy outcomes in RA patients, and evaluate impact of different therapies on the maternal and fetal health. The follow-up study will be scheduled every 4 weeks from confirmed pregnancy until delivery, records the disease activity of RA, pregnancy outcome and safety with the help of the "smart disease management system (SSDM)" and face-to-face consultations. The effects of different therapies on maternal and fetal will be valued ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05651373
Study type Observational
Source Qilu Hospital of Shandong University
Contact Qiang Shu
Phone 0086-0531-82169654
Email shuqiang@sdu.edu.cn
Status Recruiting
Phase
Start date July 30, 2021
Completion date December 31, 2024

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