IV Ibuprofen for the Prevention of Post-ERCP Pancreatitis
试验速览
- 阶段
- 2 期
- 状态
- 终止
- 入组人数
- 69
- 试验地点
- 1
- 主要终点
- Post-ERCP Pancreatitis
研究概览
简要总结
Endoscopic retrograde cholangiopancreatography (ERCP) is an advanced endoscopic technique utilized to diagnose and treat pathologic conditions involving the ducts draining the liver and pancreas. Post-ERCP pancreatitis (PEP) is the most common complication following ERCP and occurs in approximately 11% of children undergoing the procedure. By definition it leads to prolongation of hospital stay or delays in care and rarely can result in long-term morbidity or even death. Recent adult trials have demonstrated prevention of PEP with administration of rectal nonsteroidal anti-inflammatory drugs (NSAIDS). To date, no studies have been performed in children thus no "gold standard" or even commonly accepted method of preventing PEP in the pediatric population exist. Studying an IV NSAID such as ibuprofen has distinct advantages over rectally administered NSAIDs in the pediatric population in that it would allow for more consistent weight based dosing and would have more predictable absorption compared to suppository. Thus, this project proposes a pilot study evaluating the effectiveness of IV ibuprofen at preventing PEP in the pediatric population. The design of the proposed study is a prospective randomized double-blind trial comparing IV Ibuprofen to placebo controls (normal saline) at the time of procedure in patients undergoing ERCP at Children's Medical Center Dallas over a two-year period. The primary outcome measurement will be development of PEP. Post-ERCP bleeding and change in pre- and post- procedural pain scores will also be measured. The hypothesis is that IV Ibuprofen administered at the time of ERCP will decrease rates of post-ERCP pancreatitis in pediatric patients.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- — 至 18 Years(Child, Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age<=18 years
- •Undergoing ERCP (defined as cannulation of the major or minor papilla) for any indication
排除标准
- •Pancreatitis within the 72 hours preceding ERCP
- •Allergy or hypersensitivity to Aspirin or NSAID medications
- •Pregnancy or breastfeeding mother
- •Gastrointestinal hemorrhage in preceding 72 hours
- •Heart disease reliant upon a patient ductus arteriosis
- •History of sickle cell disease
研究组 & 干预措施
Ibuprofen
Single dose IV Ibuprofen at a dose of 10mg/kg (max: 800mg).
干预措施: Ibuprofen (Drug)
Placebo
Single dose IV normal saline
干预措施: placebo (Drug)
结局指标
主要结局
Post-ERCP Pancreatitis
时间窗: 2 weeks
Number of patients who develop post-ERCP pancreatitis
次要结局
- Post-ERCP Bleeding(2 weeks)
研究者
David M Troendle
Dr.
University of Texas Southwestern Medical Center
