EUCTR2007-004222-24-DE进行中(未招募)不适用
Intra-individual, randomized comparison of the MRI contrast agents Gadovist 1.0 versus Dotarem when imaging the pelvis in patients with spondylarthritides, evaluated in a blinded read
Dekan des FB Medizin der Johann-Wolfgang Goethe-Universität0 个研究点目标入组 60 人开始时间: 2007年11月21日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Patients (> 18 yrs) with known or who are highly suspicious of having Spondylarthritides (SpA) with axial involvement and inflammatory back pain and are indicated for contrast-enhanced MRI of the pelvis
- •Patients who are willing to undergo study procedures
- •Patients who are willing and able to sign informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- ••Patients who have previously entered this study
- •Patients who are in pregnancy or nursery. In women with child bearing potential a pregnancy test must be performed directly before each MR examination in order to safely exclude pregnancy.
- •Patients with any physical or mental status that interferes with the signing of informed consent
- •Patients with a contraindication for MRI
- •Patients who have received any contrast material within 12 hours prior to injection with study, comparator or similar drug in combination with moderate or severe renal impairment.
- •Patients who require emergency treatment
- •Patients with severely impaired hepatic function (e.g. SGPT equal or more than 2 times the upper limit of reference range)
- •Patients with impaired renal function of CKD stadium 3 and higher (e.g. creatinine clearance < 60ml/ min). In patients with known renal impairment, clearance will be calculated based on serum creatinine level using the Cockroft-Gault formula. Calculation of the clearance must be done before begin of study.
- •Patients with underlying disease or concomitant medication which may interfere with efficacy evaluation
- •Patients with known anaphylactoid or anaphylactic reaction to any contrast media.
研究者
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