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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06233929
Other study ID # SYSKY-2023-1235-01
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 1, 2024
Est. completion date March 1, 2033

Study information

Verified date January 2024
Source Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 2000
Est. completion date March 1, 2033
Est. primary completion date March 1, 2033
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Patients aged 18 years or older and diagnosed with RA according to 1987 ACR or 2010 ACR / EULAR classification criteria Exclusion Criteria: - Patients diagnosis with tumors without control, or AIDS - Patients with serious disease in cardiovascular, kidney and blood and endocrine system; and 3) history of schizophrenia or epilepsy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Outcome

Type Measure Description Time frame Safety issue
Primary Myopenia Myopenia was defined by an ASMI= 7.0 kg/m2 in men and= 5.7 kg/m2 in women according to the Asian Working Group for Sarcopenia (AWGS) 10 years
Primary CVDs CVDs were defined as a verified medical history of angina pectoris, myocardial infarction, heart failure, ischemic or hemorrhagic stroke, and peripheral arterial disease [17], which was verified through a questionnaire survey and confirmation by medical record 10 years
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