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NCT Number: NCT04170504

Efficacy of Chinese Herbal Medicine Qing Re Huo Xue in Patients With Rheumatoid Arthritis

This study is a multicenter, randomized, double-blinded, placebo-controlled trial with two parallel arms. The aim of the study is to evaluate whether Chinese herbal medicine Qing Re Huo Xue (QRHX) combined with methotrexate (MTX) might be better than Qing Re Huo Xue placebo combined with MTX for patients with active rheumatoid arthritis (RA).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Guang'anmen Hospital, China Academy of Chinese Medical Sciences

Beijing, 100053, China

About this study

To compare the efficacy and safety of Chinese herbal medicine Qing Re Huo Xue (QRHX) and methotrexate (MTX) for patients with active rheumatoid arthritis (RA), a multicenter, randomized controlled trial will be conducted. Two hundred and four patients with active RA will be randomly allocated (1:1) to treatment with QRHX 10g bid and MTX 10mg once a week for 24 weeks, or MTX plus QRHX placebo. The primary outcome is the bone marrow edema score in Outcome Measures in Rheumatology Clinical Trials RA MRI Scoring (OMERACT-RAMRIS) at week 24.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject has had a confirmed diagnosis of rheumatoid arthritis according to 2010 ACR/EULAR RA classification criteria.
  • Subject has a DAS28 CRP disease activity score of >3.2 at screening.
  • Subject also experienced the following signs and symptoms: swelling, joint pain, and heat in the joints.
  • Subject has had no prior exposure to oral glucocorticoids at a daily dose greater than 10 mg or to any biologic agents.
  • Subject may has had previous exposure to nonsteroidal anti-inflammatory drugs (NSAIDs) prior to screening and must be on stable dose.

Exclusion criteria

  • History or presence of a clinically significant medical disorder other than RA that, in the opinion of the investigator and medical monitor, would pose a risk to subject safety or interfere with the study evaluation, procedures, or completion.
  • Subject has inflammatory, rheumatological disorders other than RA, where arthritis may be a prominent feature.
  • Subject has received treatment with the prohibited therapies listed in the protocol, or changes to those treatments, within the prescribed timeframe.
  • Pregnant or nursing an infant or with a life partner who is pregnant, nursing, or planning to become pregnant.

Treatment and study plan

Qing Re Huo Xue (QRHX) granule

Drug

Qing Re Huo Xue (QRHX) granule 10g bid for 24 weeks

methotrexate

Drug

Oral methotrexate 10 mg per week for 24 weeks.

Other names: XINYI Pharm

Qing Re Huo Xue (QRHX) granule placebo

Drug

Qing Re Huo Xue (QRHX) granule placebo 10g bid for 24 weeks

Primary outcomes

  1. Change in bone marrow edema score from baseline at week 24 in OMERACT RAMRIS

    Time frame: week 0, week 24

    Bone marrow edema score will be assessed by OMERACT-RAMRIS scoring system; minimum value: 0, maximum value: 75; higher scores mean a worse outcome.

Secondary outcomes

  1. Change in bone erosion score from baseline at week 24 in OMERACT RAMRIS

    Time frame: week 0, week 24

    Bone erosion score will be assessed by OMERACT-RAMRIS scoring system; minimum value: 0, maximum value: 250; higher scores mean a worse outcome.

  2. The proportion of participants with no progression in bone marrow edema and bone erosion

    Time frame: week 24

    No progression in bone marrow edema and bone erosion at week 24 is defined as change in RAMRIS osteitis/erosion score ≤0.

  3. The proportion of participants achieving ACR response (ACR20, ACR50, ACR70)

    Time frame: week 4, week 12, week 24

    The proportion of participants achieving ACR response (ACR20, ACR50, ACR70)

  4. Change in the 28-joint Disease Activity Score in erythrocyte sedimentation rate

    Time frame: week 0, week 4, week 12, week 24

    The improvement of DAS28-ESR and proportion of subjects achieving remission was completed. The subjects achieving remission will be defined as DAS28-ESR <2.6.

  5. Change in Clinical Disease Activity Index (CDAI)

    Time frame: week0, week4, week 12, week 24

    The improvement of CDAI and proportion of subjects achieving remission was completed. The subjects achieving remission will be defined as CDAI <2.8.

  6. Change in Chinese patient-reported activity index with rheumatoid arthritis (CPRI-RA)

    Time frame: week0, week 4, week 12, week 24

    CPRI-RA,The self-rating scale consists of 11 items,Each item was rated 0, 1, 2 and 3 on the scale of asymptomatic to aggravating symptoms, respectively.

  7. Change in Health Assessment Questionnaire Disability Index (HAQ-DI)

    Time frame: week0, week4, week 12, week 24

    The self-rating scale consists of 20 items,Each item was rated 0, 1, 2 and 3 on the scale of asymptomatic to aggravating symptoms, respectively. (range: 0 [best] to 3 [worst])

Sponsors and collaborators

Lead sponsor

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

Other

Registry information

Official study title

Efficacy of Chinese Herbal Medicine Qing Re Huo Xue in Patients With Rheumatoid Arthritis: A Randomized Controlled Trial

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Nov 20, 2019
Registry last updated
Sep 23, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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