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A Clinical Study of Xin'an Medicine in the Treatment of Bi Syndrome

Efficacy and Safety of Xinfeng Capsule in the Treatment of Rheumatoid Arthritis (RA):A Randomized, Double-blind, Double-dummy, Multi-center Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01774877
Enrollment
304
Registered
2013-01-24
Start date
2013-07-31
Completion date
2014-08-31
Last updated
2014-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rheumatoid Arthritis

Keywords

xinfeng capsule;, rheumatoid arthritis (RA);, randomized;, double-blind;

Brief summary

Bi Syndrome is one of Traditional Chinese Medicine(TCM)name, It means an obstruction in Chinese,and it refers the syndrome characterized by the obstruction of qi and blood in the meridians due to the invasion of external pathogenic wind,cold and dampness, manifested as soreness, pain, numb,etc. Bi Syndrome contains Rheumatoid arthritis(RA). RA is a chronic disease affecting more than 20 million people in the world.It is one of the most common forms of autoimmune disease. Xin'an Medicine is one of Traditional Chinese Medicine which originated from AnHui. Xinfeng Capsule developed according to the Xin'an medicine theory ,and it has long been adopted for treatment of rheumatoid arthritis (RA). The study is aimed to evaluate the effectiveness and safety of Xinfeng Capsule in the treatment of RA.

Interventions

Xinfeng capsule:Three each time, 3 times a day, Oral,for 3 months; placebo(for leflunomide):10mg each time, 1 time a day, Oral,for 3 months; Participants will continue on the stable dose of glucocorticoids and NSAIDs that they were receiving prior to study entry

DRUGleflunomide

leflunomide :10mg each time, one time a day, Oral,for 3 months; placebo(for xinfeng capsule):Three each time, 3 times a day, Oral,for 3 months; Participants will continue on the stable dose of glucocorticoids and NSAIDs that they were receiving prior to study entry

Sponsors

Ministry of Science and Technology of the People´s Republic of China
CollaboratorOTHER_GOV
The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of RA, classified by American Rheumatism Association 1987 revised criteria. * According with the Zheng diagnosis of Traditional Chinese Medicine. * age from 18 to 65 years. * For patients currently receiving non-steroidal anti-inflammatory drugs (NSAIDs): Treatment at a stable dose during last 4 weeks prior to screening,or Patients do not take NSAIDs at least 1 weeks prior to screening. * Patients not taking DMARDs at least 4 weeks prior to screening. * Patients taking corticosteroids (≤15mg prednisone or Equivalent) ≥4 weeks before entering the trial. * Patients agree to participate in this study and sign the informed consent form.

Exclusion criteria

* Patients have received intra-articular or systemic corticosteroid injection within 4 weeks of screening. * Patients have high disease activity (DAS28-3 scores\> 5.1). * Patients have diagnosed any other chronic inflammatory disease or connective tissue disease like sicca syndrome(SS), systemic lupus erythematosus (SLE)etc; * Patients with sever diseases in Cardiovascular, brain, lung, liver, kidney and hematopoietic system ; * Patients who are pregnant or nursing mothers or Psychiatric patients. * Patients with active gastroduodenal ulcer or gastritis which caused by long-term use of NSAIDs; * The patient who has known hypersensitivity to trial medicine . * Patients have participated in other clinical trials within 4 weeks of screening.

Design outcomes

Primary

MeasureTime frameDescription
ACR20 (American College of Rheumatology (ACR) criteria of 20% improvement in symptoms )baseline,week4,week8,week12ACR20 used for evaluating the efficacy of rheumatoid arthritis (RA).

Secondary

MeasureTime frameDescription
ACR70 (American College of Rheumatology (ACR) criteria of 70% improvement in symptoms )baseline,week4,week8,week12ACR50 used for evaluating the efficacy of rheumatoid arthritis (RA).
Patterns based on Chinese medicine(CM)symptomsbaseline,week4,week8,week12
Disease Activity Scale (DAS)28baseline,week4,week8, week12
ACR50 (American College of Rheumatology (ACR) criteria of 50% improvement in symptoms )baseline,week4,week8,week12ACR50 used for evaluating the efficacy of rheumatoid arthritis (RA).
Life Quality Assessmentbaseline,week12Life Quality Assessment,including Health Assessment Questionnaire (HAQ), Self-rating depression scale(SDS), Self-rating anxiety scale(SAS),quality of life Questionnaire with rheumatoid arthritis.
x-rays of the hands and wristsbaseline,week12
Rheumatoid arthritis (RA) biomarkersbaseline, week12Rheumatoid arthritis (RA) biomarkers,including rheumatoid factor (RF), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP) ,anti-cyclic citrullinated peptide (anti-CCP) antibodies, IgG、IgA、IgM, d-dimer, the coagulation function tests

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 22, 2026