EUCTR2008-002958-37-IT进行中（未招募）不适用
Differences in dynamic contrast-enhanced (DCE) MRI measurements using Magnevist (Gd-DTPA) and Vas-ovist in patients with untreated squamous cell cervical carcinoma. - ND
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
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
- Female
入选标准
- •Adult patients (18 years and older)
- •Patients willing and able to undergo all study procedures
- •Patients affected by untreated histologically diagnosed SCCC.
- •Patients who have signed the written 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) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •History of severe allergic reaction or allergic reaction to MR contrast media.
- •Pregnant or lactating women.
- •Not being able to remain lying down for at least 45-60 min (e.g., patients with dyspnea at rest, severe pain at rest, severe back pain).
- •Patients with a contraindication to MRI such as pacemaker, aneurysm clip, or severe claustrophobia.
- •Uncooperative patients, in the investigator?s opinion.
- •Patients affected by severe renal impairment (GFR<30mL/min/1.73m2).
- •Patients participating in another clinical trial.
研究者
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