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Rheumatoid Arthritis Real-world Cohort Study in China (ReALSA) - Trial NCT06233929

Access comprehensive clinical trial information for NCT06233929 through Pure Global AI's free database. This phase not specified trial is sponsored by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University and is currently Not yet recruiting. The study focuses on Rheumatoid Arthritis. Target enrollment is 2000 participants.

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NCT06233929
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Trial Details
ClinicalTrials.gov โ€ข NCT06233929
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Rheumatoid Arthritis Real-world Cohort Study in China (ReALSA)

Study Focus

Rheumatoid Arthritis

Observational

Sponsor & Location

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Timeline & Enrollment

N/A

Mar 01, 2024

Mar 01, 2033

2000 participants

Primary Outcome

Myopenia,CVDs

Summary

An ongoing long-term cohort study is conducted in the Sun Yat-sen Memorial Hospital of Sun
 Yat-sen University, that is dedicated to recruiting RA patients, to identify the development
 of clinical, neuroimaging, and biochemical biomarkers for the diagnosis and prognosis of RA,
 especially for those with sarcopenia/myopenia
 
 To improve the prognosis of RA, this study includes the following objectives:
 
 1. Construct a useful database to explore the secular dynamic progress of RA, especially
 the difference between early and lately RA, as well as to improve our understanding of
 the life-course factors affecting the process that will facilitate future research
 activities.
 
 2. Identify the potential markers (clinical, biomedical and imaging) affecting/predicting
 the development process of sarcopenia/myopenia or other prognosis in RA patients.
 
 3. Develop the related multi-modal prediction models with clinical, biomedical and imaging
 variables to improve the diagnosis and prognosis of RA.

ICD-10 Classifications

Rheumatoid arthritis, unspecified
Other rheumatoid arthritis
Other specified rheumatoid arthritis
Rheumatoid arthritis with involvement of other organs and systems
Seronegative rheumatoid arthritis

Data Source

ClinicalTrials.gov

NCT06233929

Non-Device Trial