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Rheumatoid Arthritis (RA)NCT07484243

Clinical Cohort Construction and Therapeutic Effect Evaluation of Integrated Traditional Chinese and Western Medicine in the Treatment of Rheumatoid Arthritis

An observational study of Rheumatoid Arthritis (RA) and Rheumatoid Arthritis-Associated Interstitial Lung Disease, run by Dongyi He at 1 site in China.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This is a large-scale, multicenter observational study on the treatment of rheumatoid arthritis (RA) with integrated Traditional Chinese and Western medicine. The study plans to enroll at least 10,000 patients, including a minimum of 1,000 cases with difficult-to-treat RA (D2T RA) and 1,000 cases with RA-associated… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Integrated Traditional Chinese and Western Medicine
How many people
10,000 participants
Where
1 siteChina
Study dates
22 Aug 2025to 31 Mar 2029
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Rheumatoid arthritis patients from outpatient or inpatient departments of the participating hospital centers in this study.

Who may be able to join

  • Meet the RA classification criteria established by ACR in 1987 or the revised RA diagnostic criteria by ACR/EULAR in 2010;
  • D2T-RA must comply with the D2T-RA diagnostic criteria by ACR/EULAR in 2020 or the China D2T-RA diagnostic criteria in 2021;
  • RA-ILD patients require joint evaluation by rheumatologists and pulmonologists, with a clear diagnosis of ILD and exclusion of other possibilities such as pneumoconiosis, allergic alveolitis, idiopathic pulmonary fibrosis, and other connective tissue disease-related interstitial lung diseases (CTD-ILD);
  • Traditional Chinese medicine syndrome differentiation standards refer to the "Guidelines for Diagnosis and Treatment of Rheumatoid Arthritis" by the China Association of Chinese Medicine, the "Clinical Research Guidelines for New Traditional Chinese Medicine Drugs" by the National Medical Products Administration, and the "Diagnostic and Therapeutic Criteria for Traditional Chinese Medicine Diseases" by the Institute of Clinical Research of the China Academy of Chinese Medical Sciences;
  • Receive traditional Chinese medicine treatment;
  • Age ≥18 years;
  • Sign an informed consent form.

Who cannot join

  • Severe, progressive, or uncontrolled diseases of the kidneys, liver, blood, gastrointestinal tract, endocrine system, lungs, heart, nervous system, mental health, or brain, or current known malignant tumors;
  • Known clinically significant environmental exposures that may cause pulmonary fibrosis (PF), including but not limited to dust, asbestos, beryllium, radiation, amiodarone, bleomycin, etc.;
  • Poorly controlled severe asthma or chronic obstructive pulmonary disease (COPD) with medication adjustments within 3 months prior to screening;
  • Active infections that the investigator deems may interfere with study assessment;
  • Any clinically or laboratory abnormalities deemed significant by the investigator or other reasons that disqualify participants from this clinical study.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

China1 site, 1 recruiting
  • Shanghai Guanghua Hospital of Integrative Medicine

    Shanghai, 200052

    Recruiting

Other trials in China

About this study

This is a large-scale, multicenter observational study on the treatment of rheumatoid arthritis (RA) with integrated Traditional Chinese and Western medicine.

The study plans to enroll at least 10,000 patients, including a minimum of 1,000 cases with difficult-to-treat RA (D2T RA) and 1,000 cases with RA-associated interstitial lung disease (RA-ILD). Through long-term follow-up, data will be collected on Traditional Chinese Medicine (TCM) syndrome characteristics, treatment plans, adverse drug reactions, and complications. Biological samples, including blood and urine, will also be collected.

Read more

The research will utilize multi-omics technologies such as genomics and proteomics, combined with clinical data, to deeply explore the modern scientific connotation of the "disease-syndrome-symptom" framework in RA. The goal is to clarify the patterns and advantages of TCM syndrome differentiation and treatment. Based on these findings, a scientific and standardized efficacy evaluation system for integrated treatment will be established, and optimized treatment strategies for D2T RA and RA-ILD will be developed.

The project is led by multiple national TCM clinical research centers and regional diagnostic and treatment centers, including the First Teaching Hospital of Tianjin University of TCM and Shanghai Guanghua Hospital of Integrated Traditional Chinese and Western Medicine. These institutions have mature clinical research platforms, biobanks, and databases, providing a solid foundation for the successful implementation of this study.

The results of this research will provide a scientific basis for the integrated treatment of RA, promote the standardization of diagnostic and treatment protocols, and ultimately improve the overall level of RA prevention and treatment in China.

Read the detailed description
  1. Study Overview Rheumatoid arthritis (RA) is an autoimmune disease primarily characterized by erosive arthritis. Under the guidance of Traditional Chinese Medicine (TCM) syndrome differentiation theory, integrated treatment with TCM and Western medicine has demonstrated significant clinical benefits in managing difficult-to-treat RA (D2T RA) and RA-associated interstitial lung disease (RA-ILD). However, the biological association between RA phenotypes and TCM syndromes remains unclear, and the modern medical material basis of the "disease-syndrome-symptom" framework requires further elucidation. Therefore, employing a "disease-syndrome combination" approach to identify key biomarkers and core syndromes in RA pathogenesis, and to clarify the advantages of integrated treatment strategies, will provide a theoretical foundation for systematic research on RA diagnosis and treatment laws in integrated medicine. Building upon previous research, this study will enroll at least 10,000 patients in a multicenter cohort receiving integrated TCM and Western medicine treatment for RA, including no less than 1,000 patients with D2T RA and no less than 1,000 patients with RA-ILD. Data to be collected include TCM syndrome characteristics, clinical profiles, treatment regimens, adverse drug reactions, biological samples, complications, and follow-up information. Through systematic data collection and analysis, the study aims to establish a multicenter research cohort biobank and clinical database for integrated RA treatment. By summarizing clinical diagnosis and treatment patterns and integrating multi-omics research data, the study will further explore the modern scientific material basis of D2T RA and RA-ILD within the "disease-syndrome-symptom" framework. The research will focus on elucidating the advantages and patterns of TCM syndrome-based treatment in RA and establishing a scientific, standardized efficacy evaluation system. This study is expected to provide scientific evidence for integrated TCM and Western medicine treatment of RA, validate the unique efficacy of TCM in RA management, offer practical references for clinical practice, provide important theoretical support and practical basis for improving the overall level of RA prevention and treatment in China, and promote the standardization and normalization of integrated RA treatment.
  2. Study Objectives and Content 2.1 Study Objectives Currently, the biological association between RA phenotypes and TCM syndromes remains unclear, and the modern medical material basis of the "disease-syndrome-symptom" framework requires further elucidation. Therefore, this study aims to observe the effectiveness and safety of integrated TCM and Western medicine in the clinical treatment of RA, establish an RA clinical information database and biobank, employ a "disease-syndrome combination" approach to explore key biomarkers and core syndromes in RA pathogenesis, identify optimal integrated treatment strategies, and subsequently develop a scientific and standardized efficacy evaluation system. 2.2 Study Content This study will collect data from a multicenter cohort of 10,000 patients receiving integrated TCM and Western medicine treatment for RA, including at least 1,000 patients with D2T RA and at least 1,000 patients with RA-ILD. The main research components include the following: Collection of patient clinical data: Including TCM syndrome characteristics, treatment regimens, adverse drug reactions, complications, and follow-up status. Biological sample collection and analysis: Collecting blood, urine, and other biological samples from patients, and integrating genomics, proteomics, metabolomics and other multi-omics approaches to analyze the molecular biological characteristics of different patients. Efficacy evaluation of integrated treatment: Through controlled studies, analyzing the advantages of integrated TCM and Western medicine in RA treatment, exploring its therapeutic mechanisms, and clarifying the advantages of TCM syndrome-based treatment. Establishment of database and biobank: Through collected clinical data and biological samples, establishing a biobank and clinical database for the RA multicenter research cohort. This platform will serve as a foundation for subsequent research, supporting long-term scientific data accumulation and sharing. Elucidation of the modern scientific material basis of RA "disease-syndrome-symptom": Through integration of multi-omics data and clinical data, further exploring the scientific material basis of Wind-Damp Obstruction syndrome D2T RA and Liver-Kidney Yin Deficiency syndrome RA-ILD within the "disease-syndrome-symptom" framework, promoting the deepening of TCM modernization research. Construction of an efficacy evaluation system: Integrating clinical practice with multi-omics data to establish an efficacy evaluation system applicable to integrated TCM and Western medicine treatment of RA, ensuring scientific, standardized, and quantifiable assessment of therapeutic effects. Optimization and validation of integrated treatment protocols: By analyzing the effects of different treatment components, identifying and validating the advantageous components in D2T RA and RA-ILD integrated treatment protocols, forming treatment protocols with therapeutic advantages, and providing theoretical support for future clinical treatment.
  3. Existing Facilities and Sample Resources The First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, as the primary leading institution of this project, is a National Medical Center (TCM), a National Clinical Research Center for TCM, a Regional TCM Diagnosis and Treatment Center of the National Administration of Traditional Chinese Medicine, and a Key Laboratory of the National Administration of Traditional Chinese Medicine. It has undertaken and successfully completed the National Key Research and Development Program project "Optimization of TCM Protocols and Construction of Decision Platform for Rheumatoid Arthritis," which passed acceptance and provides platform support for optimizing TCM protocols for RA. The institution has undertaken more than twenty projects including National Key Research and Development Programs and National Natural Science Foundation projects, and has received more than ten national and provincial/ministerial-level awards, including a National Science and Technology Progress Second Prize.

Shanghai Guanghua Hospital of Integrated Traditional Chinese and Western Medicine, as the primary enrolling institution, is a Regional Diagnosis and Treatment Center of the National Administration of Traditional Chinese Medicine and a National Superior Specialty of TCM. It was nominated in the Rheumatology category of the 2023 Fudan Version Specialty Reputation Ranking. Previously, the hospital established a cohort of over 8,000 RA patients receiving integrated treatment and a cohort of over 5,000 RA-ILD patients receiving integrated treatment. Professor Chen Zhicai, a Shanghai renowned TCM practitioner, created the Quyu Qingfei Formula for treating RA-ILD, and basic and clinical research have confirmed its effectiveness and safety. This achievement received the Shanghai Integrated Traditional Chinese and Western Medicine Science and Technology Third Prize. In the past five years, the hospital has published over 80 SCI papers with a total impact factor of 241.61, including 4 papers with impact factors above 10, and 4 papers selected in the TOP100 of high-value papers in the field of Rheumatology and Immunology in China for 2022. The hospital is affiliated with the Institute of Joint Diseases of Shanghai Academy of Traditional Chinese Medicine, implementing an integrated hospital-institute management model, providing a complete clinical-research-translation integrated development platform for the advancement of rheumatology and immunology disciplines. The institute possesses an intelligently information-managed biobank and clinical database, with 20,000 RA biological samples in storage, including whole blood, plasma, serum, blood cells, synovium, and cartilage, providing abundant clinical resources for the research team.

Furthermore, in collaboration with multiple clinical institutions including Huashan Hospital Fudan University, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine affiliated with Shanghai University of Traditional Chinese Medicine, Henan Provincial Hospital of Traditional Chinese Medicine, and Guangxi Medical University, the research team possesses adequate research foundation conditions.

Being tested
Integrated Traditional Chinese and Western Medicine
Medical subject headings
Arthritis, Rheumatoid

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Integrated Traditional Chinese and Western MedicineDrug

    Integrated Traditional Chinese and Western Medicine

  • Integrated Traditional Chinese and Western MedicineOther

    Integrated Traditional Chinese and Western Medicine

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. DAS28-ESR at each time point

    The European League Against Rheumatism (EULAR) proposed the mean disease activity score (DAS28) of 28 joints as the efficacy evaluation index for rheumatoid arthritis (RA) disease activity: DAS28 = 0.56*SQRT(T28) + 0.28*SQRT(SW28) + 0.70*Ln(ESR) + 0.014*VAS

    Measured: Efficacy was assessed at weeks 0, 12,24,36, and 52.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Mar 2026
  2. Study start22 Aug 2025
  3. Primary completion30 Sep 2028 (estimated)
  4. Study completion31 Mar 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
10,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07484243
Sponsor's protocol ID
2024-K-115
Status last verified
Mar 2026
First submitted
16 Mar 2026
Last updated
21 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: all IPD that underlie results in a publication

Questions about this trial

What is this clinical trial studying?

An observational study of Rheumatoid Arthritis (RA) and Rheumatoid Arthritis-Associated Interstitial Lung Disease, run by Dongyi He at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 21 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Dongyi He (15800300800, ghyykyk@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

DAS28-ESR at each time point (time frame: Efficacy was assessed at weeks 0, 12,24,36, and 52.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Jul 2026.

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