NL-OMON39343尚未招募4 期
Magnetic Resonance Imaging to diagnose endometriosis using Ablavar ® as contrast agent - a feasibility study - Ablavar ® in endometriosis diagnosis
Medisch Universitair Ziekenhuis Maastricht0 个研究点目标入组 5 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 5
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
- •Older that 18 years;
- •Suspect of peritoneal endometriosis, palpable nodule at physical examination;
- •Patient planned for MRI and laparoscopic treatment of the disease;
- •Pre menopausal;
- •Using contraception during the time of the study;
- •Willing and able to undergo all study procedures;
- •written informed consent.
排除标准
- •Pregnancy / breast feeding;
- •Post menopausal status or under GnRH analogue treatment;
- •Patients presenting with a contraindication to MRI such as pacemaker, aneurysm clip, severe claustrophobia or ferromagnetic implants;
- •Impaired kidney function (estimated Glomerular Filtration Rate, eGFR < 60) or acute kidney injury;
- •History of severe allergic reaction or allergic reaction to MR contrast media;
- •Allergy (hypersensitivity) to any of the ingredients of Ablavar ®;
- •Being unable to give informed consent in person.
研究者
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