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Clinical Trial Summary

The purpose of this study is to access the effect (week 12/week 24) of puerarin injection on carotid intima-media thickness (CIMT) in rheumatoid arthritis (RA) patients despite routine anti-rheumatic treatment.


Clinical Trial Description

- Controlled, randomized trial

- RA patients under routine anti-rheumatic care were randomized to receive the treatment with or without 400 mg puerarin injection

- Assessments were made at entry, 12 and 24 weeks

- The overall sample size was assessed before the enrollment

- Randomization was performed using concealed random allocation method

- The collected data was processed and assessed by two reviewers

- All the measurement and analysis procedures concerning CIMT were performed by a single ultra sonographer and a single reader, who were blinded to patient profiles and group assignment

- The reproducibility of the ultrasonographic method was test before the trial ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02254655
Study type Interventional
Source Chengdu PLA General Hospital
Contact
Status Completed
Phase Phase 2
Start date November 2013
Completion date November 2017

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