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临床试验/NCT01818050
NCT01818050Unknown4 期

Prospective Evaluation of Stent Patency in Patients With Benign Biliary Obstruction of the Wing Biliary Stent (Viaduct™)

Stanford University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2013年3月最近更新:
适应症

试验速览

阶段
4 期
入组人数
50
试验地点
2
主要终点
Biliary stent patency

研究概览

简要总结

Endoscopic retrograde cholangiopancreatography (ERCP) with plastic stent placement for resolution of biliary obstruction has been the method of choice for many years. However, stent clogging/obstruction is a major limitation in the management of biliary obstruction. Studies have shown that the conventional tubular type polyethylene stents (CS) with side holes accumulate significant sludge and their mean patency is approximately 90 days.

Thus patients requiring longer term stenting need to undergo stent exchanges every 2-3 months.

Recently, a stent with a star-shaped cross-section has been developed for biliary applications. This FDA approved biliary Wing stent (WS) (ViaDuct™) is a novel plastic biliary stent that lacks a lumen, and is designed to allow bile to flow on the outside of the stent. The stent which is star shaped in cross section, channels fluid along its winged perimeter. It has been proposed that the winged stent design with a lack of central lumen obviates the risk of luminal occlusion and that the risk of occlusion, given the presence of multiple external drainage channels, is smaller. Longer term biliary drainage without the need for stent exchange should therefore be possible with these stents.

The primary aim of this study is to prospectively evaluate the patency rate of the WS up to 90 days in 50 patients with biliary obstruction due to stones or benign strictures.

详细描述

  1. Fifty patients that meet all the inclusion criteria and have none of the exclusion criteria will be invited to participate in the study.
  2. Initial visit:
  • Written informed consent will be obtained
  • Complete history and physical will be performed and the patients baseline liver function tests and imaging results will be assessed and noted in the case report form.
  • Patients gender, date of birth, concomitant medications will be noted.
  1. Procedure:

Patients will then be scheduled for the ERCP procedure with wing biliary stent placement. They will undergo the ERCP as standard of care and the wing biliary stent will be placed for decompression of the obstructed biliary system in situations where stenting is standard of care. One or more biliary stents may be placed during the procedure depending on the indication such as a biliary stricture necessitating multiple stent placements for dilation as the standard of care. 4. Bloodwork:

Patients will undergo bloodwork (total and direct bilirubin, alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase) one week after the procedure. The degree of drop in bilirubin will also be noted. The patients will be then have these labs drawn again at 4, 8 and 12 weeks after the procedure. 5. Telephone calls:

The patients will be called on the telephone at weeks 2, 4, 6, 8, 10 after the procedure to monitor their clinical status. Patients and family members will be given a contact number to call us immediately if they develop any signs of biliary obstruction such as fever, abdominal pain, jaundice, dark urine or light stools. They will also be instructed to come to the emergency room should they develop fevers. 6. Stent removal:

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients age 18 or older referred for ERCP for biliary obstruction from stones or benign strictures that have been confirmed based on clinical, laboratory and imaging findings, with an indication for plastic stent placement.
  • One or more biliary stents may be placed during the procedure depending on the indication such as a biliary stricture necessitating multiple stent placements for dilation as the standard of care.
  • Expected patient survival of at least 90 days
  • High likelihood of patient follow-up
  • Patient is able to give a written informed consent
  • Patient is willing and able to comply with the study procedures.

排除标准

  • Patients with cholangitis
  • Patients with bile leak
  • Pregnant patients
  • Patients with any contraindication to endoscopic procedure
  • Participation in another investigational study that may directly or indirectly affect the results of this study within 30 days prior to the initial visit
  • Patients with malignant biliary strictures

结局指标

主要结局

Biliary stent patency

时间窗: At 90 days after stent placement

次要结局

  • Liver Function Test improvement(90 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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