ACTRN12623000420640招募中1 期
The Feasibility and Pharmacokinetics of Intensive Therapy for Rheumatoid Arthritis using Methotrexate Loading: A 6-week randomised clinical trial.
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 85 Years(—)
- 性别
- All
入选标准
- •Patients attending the rheumatology clinic at the Central Adelaide Local Health Network (CALHN) who have active rheumatoid arthritis and for whom the decision has been made to commence methotrexate (and sulfasalazine and hydroxychloroquine) as triple DMARD therapy.
- •The decision to use methotrexate is not part of this trial. It will be made according to clinical need and according to our standardised inclusion criteria for commencement of methotrexate therapy. These include:
- •1) ALT < 2x ULN
- •2) Calculated Creatinine Clearance > 60 mL/min (Cockcroft-Gault)
- •3) Neutrophils within normal range
- •4) If a smoker, Pulmonary Function Tests will be conducted, and they must have FVC>70% predicted and DLCO> 60% predicted
- •5) At least 5 years since treatment for a malignancy (except non-melanoma skin cancers)
- •6) Not pregnant (test is done as standard prior to MTX commencement)
- •7) Able to read English and/or good communication skills.
- •8) Age greater than or equal to 18 years
排除标准
- •1) BMI < 18 because sub-cutaneous injections of MTX will be used in the loading dose group. An upper BMI was discussed but there is no apparent reason for specifying an upper limit.
- •2) Age > 85 years
研究者
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