Construction of Clinical Model of Primary Sjogren's Syndrome Combined Traditional Chinese and Western Medicine

China-Japan Friendship Hospital1,000 enrolled

Overview

This study aims to establish a large sample cohort of patients with primary sjogren's syndrome, collect multi-omics information of patients with primary sjogren's syndrome, and construct disease diagnosis model and disease prognosis prediction model.

Study Type

OBSERVATIONAL

Enrollment

1,000

Conditions

Primary Sjögren Syndrome

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Meets the 2002 AECG or 2016 ACR/EULAR classification criteria of primary Sjögren's syndrome. Exclusion Criteria: * Comorbid connective tissue disease other than the disease under research. * Women who are pregnant or breastfeeding. * Combined severe cardiovascular or cerebrovascular disease, hepatic or renal failure, or severe malignant tumors. * Other conditions (e.g., cognitive impairment) that the investigators consider ineligible for enrollment.

Locations (1)

Jiaqi Chen

Beijing, Beijing Municipality, China

RECRUITING

Outcomes

Primary Outcomes

Number of participants with system involvement

System involvement determined from clinical diagnosis

Time frame: Baseline , 6 months follow-up

Secondary Outcomes

Mortality

All-cause mortality

Time frame: Baseline , 6 months follow-up

Number of participants with tumor

Tumor determined from clinical diagnosis

Time frame: Baseline , 6 months follow-up

Number of participants with connective tissue disease

Connective tissue disease determined from clinical diagnosis

Time frame: Baseline , 6 months follow-up

Data from ClinicalTrials.gov

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