NL-OMON45561已完成不适用
Quantitative kinetic analysis of [11C]DPA-713 and [18F]PEG-Folate uptake in joints of patients with rheumatoid arthritis - [11C]DPA-713 and [18F]PEG-Folate in rheumatoid arthritis
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 6
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •* Men and women, * 18 years of age.
- •* Diagnosis of rheumatoid arthritis according to the 1987 revised criteria of the American Rheumatism Association (ARA) and/or the 2010 ACR/EULAR Rheumatoid Arthritis Classification Criteria.
- •* Patients with obvious clinical arthritis activity assessed by a physician, in at least 1 hand, wrist of knee joints.
- •* Treatment with disease modifying anti-rheumatic drugs (DMARDS), biologics and oral corticosteroids up to 10 mg daily is allowed. Non-steroidal anti-inflammatory drugs (NSAID) is permitted, provided that there is a stable dose for at least 1 month.
- •* Patients must be able to adhere to the study appointments and other protocol requirements.
- •* Patients must be capable of giving informed consent and the consent must have been obtained prior to the study related procedures.
排除标准
- •* Use of intramuscular or intravenous corticosteroids within 4 weeks prior to screening.
- •* Treatment with any investigational drug within the previous 3 months.
- •* Pregnancy or breast-feeding
- •* Anemia (Hemoglobine <6.0 mmol/L)
- •* Renal insufficiency (GFR <30 mL/min/1.73m2)
研究者
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