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临床试验/NL-OMON45561
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

Vrije Universiteit Medisch Centrum0 个研究点目标入组 6 人开始时间: 待定最近更新:
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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