NL-OMON44776已完成3 期
A randomized clinical trial investigating LanreotIde For output reduction in patients with high-output Enterocutaneous fistula or enterostomie - LIFE study
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 40
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
- •All adult patients with a high-output fistula (> 500ml/day) or high-output enterostomie (<1500 ml/day) after gastro-intestinal, abdominal wall surgery will be registered from the moment are referred to our multi-disciplinary outpatient treatment team. ;Inclusion criteria for randomization:
- •In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- •* Adult patients minimal 4 weeks after abdominal surgery
- •* Received minimal 2 weeks standard treatment
- •* High output small bowel fistula (>500ml/day) or enterostomy (>1500ml/day) for at least 3 consecutive days.
- •* The diagnosis of fistula origin and localization confirmed by CT/fistulography/ enteral contrast MRI.
排除标准
- •Exclusion criteria
- •A potential subject who meets any of the following criteria will be excluded from participation in this study:
- •* Treatment with short-acting somatostatin (or analogues) in the last 2 weeks or with a long-acting somatostatine analogue in the last 2 months.
- •* Patients with high output pancreatic fistula after pancreatitis
- •* Patients with symptomatic gallbladder disease
研究者
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