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临床试验/NCT02241512
NCT02241512终止2 期

IV Ibuprofen for the Prevention of Post-ERCP Pancreatitis

University of Texas Southwestern Medical Center1 个研究点 分布在 1 个国家目标入组 69 人开始时间: 2014年9月最近更新:
适应症
干预措施
相关药物

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

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

Experimental

Single dose IV Ibuprofen at a dose of 10mg/kg (max: 800mg).

干预措施: Ibuprofen (Drug)

Placebo

Placebo Comparator

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

申办方类型
Other
责任方
Principal Investigator
主要研究者

David M Troendle

Dr.

University of Texas Southwestern Medical Center

研究点 (1)

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