- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07627893
Complementary Herbal Approach to Rheumatoid Management Study (CHARMS) (CHARMS)
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
From the Traditional Chinese Medicine (TCM) perspective, RA is part of the Bi Syndrome. Si Miao Xiao Bi Tang is one of the formulas listed in the guidelines for treatment of Damp-Heat syndrome. Till date, few studies have explored use of CHM, in particular Si Miao Xiao Bi Tang, in treating RA. According to past systematic reviews of radnomised controlled trials performed on Chinese herbs in RA patients, most studies were of low methodological quality and small numbers, resulting in lack of generalizability. Studies looking into cost effectiveness are also lacking.
Proposed project is a randomised double-blind placebo-controlled trial to be conducted over a period of three years, anchored to the Consolidated Standards of Reporting Trials (CONSORT) guidelines and CONSORT extension for CHM. Eligible patients will be randomly allocated to receive CHM and methotrexate or methotrexate and placebo on a 1:1 basis via random permuted block randomization.
Intervention group and control group patients receive methotrexate and CHM or methotrexate and placebo respectively for 12 weeks. They will attend rheumatologist reviews at weeks 0, 4, 8, and 12, including physical exams and disease monitoring. Safety is tracked through blood tests, and further tests are ordered as needed. TCM physicians participate by counselling and diagnosing TCM syndrome and monitoring for side effects during study visits at weeks 0, 4, 8 and 12.
American College of Rheumatology 20% improvement criteria (ACR20) at week 8 is the primary outcome. To achieve an ACR20 response, a patient with RA must demonstrate a 20% improvement in both tender and swollen joint counts, and 20% improvement in at least three of the following five criteria: patient's assessment of disease activity, physician's assessment of treatment response, patient's ability to perform daily activities based on Health Assessment Questionnaire-Disability Index (HAQ-DI), pain level, and serum inflammation markers.
Secondary outcomes include ACR20 response ACR50 response, ACR70 response, 28-joint disease activity score using ESR (DAS28-ESR), impact of RA on disability as measured using the Health Assessment Questionnaire Disability Index (HAQ-DI), severity of synovitis as determined using the EULAR-OMERACT ultrasound scoring system, quality of life as measured using the Medical Outcomes Study Short-Form (36-item) Health Survey (SF-36), fatigue level as measured using the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) scale and safety of the trial.
Exploratory outcome is improvement in ultrasound inflammation at week 8 as compared to baseline, based on EULAR-OMERACT ultrasound scoring system.
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 2
- Fase 3
Contactos e Locais
Contato de estudo
- Nome: Warren Fong
- Número de telefone: +65 63214028
- E-mail: warren.fong.w.s@singhealth.com.sg
Locais de estudo
-
-
-
Singapore, Cingapura, 169608
- Recrutamento
- Singapore General Hospital
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Patients between the ages of 21 and 70 years, and diagnosed with RA by a rheumatologist and fulfilling the 2010 ACR/EULAR classification criteria for RA.
- Active disease with DAS28 ESR ≥3.2 at screening, with at least 6 swollen joints out of 66 and at least 6 tender joints out of 68.
- Receiving stable doses of methotrexate therapy for at least 3 months, and on stable dose for at least 4 weeks before trial entry ( ≥10mg per week), either subcutaneous or orally.
- Stable doses of non-steroidal anti-inflammatory drugs (NSAIDS), acetaminophen, or oral corticosteroids (equivalent to prednisone ≤ 10 mg) for at least 4 weeks prior to first dose of study medication.
Except for methotrexate, patients must have discontinued all csDMARDs, including, but not limited to: hydroxychloroquine, sulfasalazine, leflunomide prior to first dose of study medication as specified below:
- ≥ 4 weeks prior to Baseline Visit for sulfasalazine and hydroxychloroquine
- ≥ 8 weeks prior to Baseline Visit for leflunomide if no elimination procedure was followed, or adhere to an elimination procedure (i.e., 11 days with cholestyramine, or 30 days washout with activated charcoal)
- A negative urine pregnancy test for women of childbearing potential on Day 1 (prior to administration of first dose of study drug).
- Use of a reliable method of contraception by all female patients of childbearing potential and male patients with procreative capacity during the study and up to 3 months after the last dose of the study medication.
Exclusion Criteria:
- Not able to provide informed consent.
- Previous lack of efficacy to Si Miao Xiao Bi Tang.
- History of inflammatory joint disease other than RA. Secondary Sjogren's Syndrome is permitted.
- Concurrent use of other immunosuppressant medications, except MTX and protocol allowed doses of steroids.
- Has been treated with intra-articular, intramuscular, intravenous, trigger point or tender point administration of corticosteroids in the preceding 4 weeks prior to the Baseline Visit.
- Subject has been treated with any investigational drug within a minimum of 30 days or five half-lives (whichever is longer) of the drug prior to the Baseline Visit or is currently enrolling in another clinical study.
- Pregnant or breastfeeding females.
- Infected with human immunodeficiency virus (HIV) or hepatitis B or C viruses, untreated malignancy, or evidence of active or untreated latent tuberculosis.
- Receipt of any live vaccine within 1 month prior to the Screening Visit, or expected need of live vaccination during study participation including up to 1 month after the last dose of study drug.
- History of clinically significant hematologic, pulmonary, renal, hepatic, or psychiatric disease that would interfere with the subject's participation in this study.
- Infection(s) requiring treatment with intravenous (IV) anti-infectives within 30 days prior to the Day 1 or oral anti-infectives within 14 days prior to the Baseline Visit.
Any uncontrolled clinically significant laboratory abnormality or any of the following laboratory abnormalities:
- Evidence of hematopoietic disorder or hemoglobin <9 g/dL
- White blood cell count <3.0 x 10^9/L (<3000/mm^3)
- Absolute neutrophil count <1.2 x 10^9/L (<1000/mm^3)
- Platelet count <100 x 10^9/L (<100,000/mm^3)
- Alanine aminotransferase (ALT), or aspartate aminotransferase (AST) greater than 1.5 times the upper limit of normal (ULN)
- Estimated glomerular filtration rate of less than 60 mL/min
- Any arrhythmia on baseline/screening ECG.
- Females of childbearing potential not willing to use contraceptive methods which, in the opinion of the investigator, are effective and adequate while on the study. Female subjects who are not of childbearing potential must meet at least one of the following criteria: (a) Have undergone a documented hysterectomy and/or bilateral oophorectomy; or (b) Achieved postmenopausal status, defined as: cessation of regular menses for at least 12 consecutive months with no alternative pathological or physiological cause.
- Been diagnosed with G6PD deficiency.
- Subjects who are taking TCM supplements regularly (daily) and not willing to stop intake.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Quadruplicar
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Intervention
In addition to usual rheumatological care, patients receive take Shu Bi Ning for a period of 12 weeks.
|
Shu Bi Ning (modified Si Miao Xiao Bi) is a chinese herbal medication for treatment of damp-heat syndrome.
Patients receive standard dose of oral methotrexate that is ordered by their attending rheumatologist.
|
|
Comparador de Placebo: Placebo
In addition to usual rheumatological care, patients receive take a Shu Bi Ning placebo for a period of 12 weeks.
|
Patients receive standard dose of oral methotrexate that is ordered by their attending rheumatologist.
Placebo granules will be manufactured with no new herbal components (all herbal content is HSA certified).
Placebo granules will comprise of 5% of the herbal components (using Modified Si Miao Xiao Bi), 95% black bean powder and 0.05% denatonium benzoate will be added as a bitterant.
This is to ensure that the placebo possesses similar taste and smell of the herbal components.
The placebo will be colour adjusted to match actual herbal granules, and the packaging for the herbal and placebo granules will be done using the same packaging material to ensure both are similar in appearance.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
American College of Rheumatology 20% improvement criteria (ACR20) at week 8
Prazo: Enrollment to week 8.
|
To achieve an ACR20 response, a patient with RA must demonstrate a 20% improvement in both tender and swollen joint counts, and 20% improvement in at least three of the following five criteria: patient's assessment of disease activity, physician's assessment of treatment response, patient's ability to perform daily activities based on Health Assessment Questionnaire-Disability Index (HAQ-DI), pain level, and serum inflammation markers.
|
Enrollment to week 8.
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
ACR20 response at week 12
Prazo: Enrollment to week 12.
|
To achieve an ACR20 response, a patient with RA must demonstrate a 20% improvement in both tender and swollen joint counts, and 20% improvement in at least three of the following five criteria: patient's assessment of disease activity, physician's assessment of treatment response, patient's ability to perform daily activities based on Health Assessment Questionnaire-Disability Index (HAQ-DI), pain level, and serum inflammation markers.
|
Enrollment to week 12.
|
|
ACR50 response at weeks 8 and 12
Prazo: Enrollment to week 8, 12.
|
To achieve an ACR50 response, a patient with RA must demonstrate a 50% improvement in both tender and swollen joint counts, and 50% improvement in at least three of the following five criteria: patient's assessment of disease activity, physician's assessment of treatment response, patient's ability to perform daily activities based on Health Assessment Questionnaire-Disability Index (HAQ-DI), pain level, and serum inflammation markers.
|
Enrollment to week 8, 12.
|
|
ACR70 response at weeks 8 and 12
Prazo: Enrollment to week 8, 12.
|
To achieve an ACR70 response, a patient with RA must demonstrate a 70% improvement in both tender and swollen joint counts, and 70% improvement in at least three of the following five criteria: patient's assessment of disease activity, physician's assessment of treatment response, patient's ability to perform daily activities based on Health Assessment Questionnaire-Disability Index (HAQ-DI), pain level, and serum inflammation markers.
|
Enrollment to week 8, 12.
|
|
28-joint disease activity score using ESR (DAS28-ESR) at weeks 8, 12.
Prazo: Enrollment to week 8, 12.
|
The DAS28-ESR is a composite measure used to evaluate disease activity in RA.
It incorporates four components: the tender joint count (TJC) and swollen joint count (SJC) out of 28 specified joints, the patient's global health assessment using a visual analog scale (VAS), and the erythrocyte sedimentation rate (ESR), which is a marker of inflammation.
The score ranges from 0 to 9.4, with thresholds defining remission (<2.6), low disease activity (2.6-3.2),
moderate disease activity (>3.2-5.1), and high disease activity (>5.1).
|
Enrollment to week 8, 12.
|
|
Impact of RA on disability as measured using the Health Assessment Questionnaire-Disability Index (HAQ-DI) at weeks 8, 12.
Prazo: Enrollment to week 8, 12.
|
The HAQ-DI is a self-reported measure of functional status.
It consists of 20 questions across eight categories: dressing and grooming, arising, eating, walking, hygiene, reach, grip, and usual activities.
Each item is scored on a scale from 0 (no difficulty) to 3 (unable to do).
The overall HAQ-DI score, ranging from 0 to 3, is calculated by averaging the eight category scores, with higher scores indicating greater disability.
|
Enrollment to week 8, 12.
|
|
Quality of life as measured using the Medical Outcomes Study Short-Form (36-item) Health Survey (SF-36) at week 8, 12
Prazo: Enrollment to week 8, 12.
|
The SF-36 measures health-related quality of life (HRQoL).
It comprises 36 questions that assesses eight health domains: physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health.
These domains can be further summarized into two component scores: the Physical Component Summary (PCS) and the Mental Component Summary (MCS).
The SF-36 uses a scoring system ranging from 0 to 100 for each domain, with higher scores indicating better health status.
|
Enrollment to week 8, 12.
|
|
Fatigue level as measured using the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) scale at week 8, 12.
Prazo: Enrollment to week 8, 12.
|
The FACIT-F is a 13-item measure designed to assess self-reported fatigue and its impact on daily activities and function.
Scores range from 0 to 52, where higher scores indicate less fatigue.
|
Enrollment to week 8, 12.
|
Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Severity of synovitis determined using the EULAR-OMERACT ultrasound scoring system at week 8
Prazo: Enrollment to week 8.
|
The EULAR-OMERACT ultrasound scoring is a standardized method for assessing synovitis, combining synovial hypertrophy (B-mode) and power Doppler signal (using semiquantitative scales from 0-3) to evaluate inflammation, developed collaboratively by the European League Against Rheumatism (EULAR) and the Outcome Measures in Rheumatology (OMERACT) group.
Higher scores indicate more severe inflammation.
|
Enrollment to week 8.
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
- Doenças musculoesqueléticas
- Artrite
- Doenças articulares
- Doenças Reumáticas
- Doenças do Tecido Conjuntivo
- Doenças autoimunes
- Doenças do sistema imunológico
- Doenças da Pele e do Tecido Conjuntivo
- Artrite, Reumatóide
- Compostos heterocíclicos
- Compostos heterocíclicos, 2 anel
- Compostos heterocíclicos, anel fundido
- Pterins
- Pteridinas
- Aminopterina
- Metotrexato
Outros números de identificação do estudo
- 2025/0161
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .