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临床试验/NCT02545153
NCT02545153Unknown2 期

Randomised Controlled Trial of Fibrin Sealant to Prevent Bile Leakage After Cholangiotomy

Lasarettet i Enköping1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2009年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
200
试验地点
1
主要终点
Postoperative biliary leakage

研究概览

简要总结

Bile leak reduction from the common bile duct, as a result of glue appliance after cholangiotomy.

详细描述

Laparoscopic common bile duct exploration is a way of dealing with common bile duct stones that has gained increasing acceptance. Following a cholangiotomy there is, however, the risk of bile leakage from the incision.

A way of avoiding leakage following cholangiotomy may be to apply fibrin sealant on the cholangiotomy.

The present study is based on patients undergoing laparoscopic cholecystectomy at the department of surgery, Enköping hospital, Sweden. The patients are informed about the study prior to the procedure. Cholangiography is performed routinely. In case common bile duct stones are encountered on the cholangiography, an incision is made in the common bile duct and the stones are extracted. After the stone extraction, a t tube is introduced into the cholangiotomy and the incision is closed with running Vicryl sutures.

When the cholangiotomy has been closed, the randomisation is performed with a sealed envelope system. If the patient is randomised to fibrin sealant, this is applied on the cholangiotomy. A passive drain is introduced before the abdomen is closed.

Postoperatively, the amount of bile in the passive drain is measured by an observer randomised to the allocation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Gallbladder disease

排除标准

  • Cancer/Tumor

研究组 & 干预措施

Fibrin sealant

Active Comparator

Tisseel, Baxter (Aprotinin and Fibrinogen)

干预措施: Tisseel, Baxter (Aprotinin and Fibrinogen) (Drug)

Control

Placebo Comparator

Suturing the incision without fibrin glue

干预措施: Control (Drug)

结局指标

主要结局

Postoperative biliary leakage

时间窗: From the the day of surgery until discharge and/or removal of abdominal drain, up to two weeks

The amount of bile in the drain is measured daily until it is withdrawn

次要结局

未报告次要终点

研究者

发起方
Lasarettet i Enköping
申办方类型
Other
责任方
Principal Investigator
主要研究者

BAHMAN DARKAHI

MD

Lasarettet i Enköping

研究点 (1)

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