Prospective Analysis of Value of Contrast-enhanced Sonography During Biopsies of Focal Liver Masses
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 入组人数
- 83
- 试验地点
- 1
- 主要终点
- Complication Rate
研究概览
简要总结
The investigators plan to compare complication and success rates between two methods of ultrasound guidance for biopsy of liver lesions, contrast-enhanced and the current protocol without contrast.
详细描述
As a major oncology and hepatology center, the investigators perform about 3-5 guided biopsies for liver tumors weekly. Ultrasound is the preferred modality for imaging biopsies due to its ability to visualize and position the biopsy needle in real time with high accuracy and safety, is nonionizing, and is quicker compared to other techniques, especially CT-guided biopsies. The failure rate of ultrasound guided liver biopsies (including cases where biopsy was declined to be performed due to lack of lesion visibility) is about 10%. By comparison, in the investigators' practice genotyping of metastatic tumors, with multiple core biopsies, is often requested for entry into oncology trials, and failure of tumor genotyping after biopsy is estimated to be about 30%.
Recently, the first ultrasound contrast agent was FDA-approved for characterization of liver lesions [sulfur hexafluoride lipid-type A microspheres (Lumason, Bracco Diagnostics, Monroe Township, NJ)]. The microbubble agent is deemed safe, including in cardiac failure patients and those with chronic airway obstruction. Injecting microbubbles may allow better visualization of lesions and adjacent vasculature by enhancing the microvasculature and adjacent vessels and potentially reduce incidence of failed biopsy or bleeding complications. In addition, determination of necrotic regions in a lesion may allow better direction of biopsy.
Yet there is limited literature on the use of ultrasound contrast agents for improving targeted liver biopsies. The investigators intend to prospectively assess the non-diagnostic biopsy and complication rates in a group of patients who undergo contrast-enhanced ultrasonography (CEUS) using microbubbles at the time of biopsy. The investigators will then compare the results from this group with the failure and complication rate from a control group of patients undergoing the standard US-guided biopsy procedure. Over 12 months the investigators expect to perform approximately 200 biopsies. Power analysis suggests that 125 patients in both contrast-enhanced sonography and control groups, each, are required. The investigators should be able to enroll sufficient patients in 18 months
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- Single (Participant)
盲法说明
Patients will not be informed of diagnostic arm.
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Males and females
- •Age 18 years or greater
- •Scheduled to undergo liver biopsy with ultrasound guidance at a performance site
排除标准
- •Liver biopsy is not intended to obtain tissue from a specific lesion
- •Known or suspected cardiac shunt
- •History of hypersensitivity to any active or inactive ingredients in Lumason
研究组 & 干预措施
biopsy with Lumason
liver biopsy performed with prior contrast enhancement with Lumason 60.7Mg Powder for Injection (experimental method)
干预措施: Lumason 60.7Mg Powder for Injection (Drug)
biopsy with placebos
liver biopsy performed without prior contrast enhancement (standard method)
干预措施: Placebos (Drug)
结局指标
主要结局
Complication Rate
时间窗: 30 days
Complication will be defined as 1) bleeding seen on post-biopsy CT or US, 2) drop in hemoglobin of more than 1.5 g/dL within one week after biopsy, or 3) need for hepatic artery embolization.
次要结局
- Success Rate(30 days)
研究者
Jordan K. Swensson
Assistant Professor Clinical Radiology
Indiana University