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临床试验/NCT02399800
NCT02399800终止不适用

Prospective Randomized Trial of EUS Guided Celiac Plexus Block for Chronic Pancreatitis

University of Southern California1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2014年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
1
试验地点
1
主要终点
Long Term CHANGE in Pain Scores

研究概览

简要总结

Rationale: Chronic pancreatitis is a chronic inflammatory disease of the pancreas which results in debilitating abdominal pain, decreased productivity and increased health care costs. Endoscopic ultrasound (EUS) guided celiac plexus block (CPB) is routinely used to treat pain related to chronic pancreatitis. While EUS guided neurolysis for pancreatic cancer has significant efficacy, the benefit of CPB for chronic pancreatitis pain is controversial and has not been studied in a rigorous manner.

Objective: To assess whether EUS guided celiac plexus block decreases suffering, hospitalization, and opiate requirements related to chronic pancreatitis pain.

Population: Patients undergoing EUS at Los Angeles County Hospital for painful chronic pancreatitis.

Methods: Patients undergoing EUS to evaluate chronic pancreatitis with a typical visual analogue pain score >3, regular opiate use, and M ANNHEIM chronic pancreatitis score >6 will be eligible.

Study Arms: Patients will be randomized to 1) diagnostic endoscopic ultrasound 2) endoscopic ultrasound with celiac plexus block

Study Outcomes: The primary outcome will be a decrease in chronic pancreatitis pain assessed by the visual analogue scale and M ANNHEIM system at 24 weeks compared to immediately prior to the block. The ability to work and conduct normal activities, opiate medication requirements, and a Careprep symptom assessment at 24 weeks will also be compared prior to the block.

Analytic Plan: The projected response rate to EUS guided CPB is 52%. Given known 30% placebo response in patients with pain related to chronic pancreatitis we anticipate that 83 patients will need to participate to demonstrate a difference. We aim to enroll 90 patients in this study.

详细描述

1.0 Background and Hypothesis: Chronic pancreatitis is an inflammatory disease of the pancreas characterized by painful scarring and loss of glandular function.The prevalence of chronic pancreatitis in the United States is estimated to be 0.2 to 5% and results in 86,000 hospitalizations. The majority of patients with chronic pancreatitis will develop significant abdominal pain which is debilitating and results in a significant burden on the health care system.

Multiple approaches, including pancreatic enzymes, narcotic analgesia, celiac plexus block and surgical ganglionectomy have been used to treat pancreatic pain with variable success. Injection of local anesthesia agents and steroids into the celiac plexus for pain control has been used for many years via both surgical and percutaneous approaches. Topical therapy theoretically prevents the conduction of painful stimuli from the pancreas and addresses inflammatory changes in the afferent nerves themselves. Splanchnic nerves pass from the pancreas to the thoracic root ganglia via the celiac ganglia which are the target for intervention. Nerve changes in chronic pancreatitis including perineural inflammation, altered diameter, and upregulation of pain neuropeptides (including Substance P) are associated with increased sensitivity to stimuli from the pancreas (distension and inflammation) as well as pain independent of stimuli (neuropathic). Endoscopic ultrasound allows for close proximity, high resolution assessment of the gastrointestinal tract wall and adjacent anatomic structures. Physicians are able to perform EUS-guided celiac plexus injections in the outpatient setting under conscious sedation. The EUS guided approach offers better visualization of the celiac region and direct access to the celiac plexus. EUS guided celiac plexus block is a core part of the routine care of patients at Los Angeles County Hospital with chronic pancreatitis. Celiac plexus block is a recommendation for refractory chronic pancreatitis pain by the European Society of Gastrointestinal Endoscopy (ESGE).

Several studies have shown that EUS-guided CPB has a beneficial role in treating pain caused by chronic pancreatitis. A randomized trial by Gress et al looked at the efficacy of EUS-guided versus CT-guided celiac plexus block for controlling abdominal pain of chronic pancreatitis in 18 patients. They found significant improvement in pain symptoms in patients randomized to EUS-guided celiac plexus block over a mean time period of 10 weeks. A study by the same group showed an improvement in overall pain score in 55% at 4 and 8 weeks of follow-up in 90 patients. Adverse events including diarrhea and infection occurred in 3%. A comprehensive review by Kaufman et al in 2010 evaluated the efficacy of EUS-guided celiac plexus block and celiac plexus neurolysis in alleviating chronic abdominal pain due to chronic pancreatitis and pancreatic cancer respectively. A total of 6 studies were included in their analysis, comprising 221 patients, and found that EUS-guided celiac plexus block was effective in 51.46% of patients with chronic pancreatitis. EUS-guided celiac plexus neurolysis (with alcohol) was effective in 72.54% of those with pancreas cancer.

These modest improvement for celiac block for chronic pancreatitis (especially in comparison to celiac plexus neurolysis in pancreas cancer) have led some investigators to question whether EUS guided celiac plexus block is an effective treatment for chronic pancreatitis pain despite its routine use. Prospective randomized controlled studies examining the efficacy of endoscopic ultrasound guided celiac plexus block are lacking.

2.0 Objectives and Purpose Our aim is to perform a pilot randomized trial to gauge the degree to which celiac plexus block performed under endoscopic ultrasound guidance will benefit patients with chronic pancreatitis. We will assess whether celiac plexus block significantly decreases pain scores, hospitalization, and pain medication requirements and increases the ability to return to normal activities.

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
Double (Participant, Outcomes Assessor)

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

  • Presentation with upper abdominal pain suggestive of pancreatitis who are undergoing EUS for evaluation
  • M ANNHEIM severity index of 6 or greater to be included
  • Intermittent episodes of pain>3 requiring opiate medication

排除标准

  • Patients who have allergic reactions to steroids or bupivacaine
  • INR >1.6
  • platelets <75
  • decompensated cirrhosis
  • incarcerated
  • <18 years old
  • unable to give informed consent
  • peptic ulcer disease
  • ongoing substance or alcohol use

研究组 & 干预措施

EUS with Celiac Block

Experimental

Celiac Block with triamcinolone and bupivicaine Intra Plexus Triamcinolone and Bupivicaine Injection

干预措施: Celiac Block with triamcinolone and bupivicaine (Procedure)

EUS with Celiac Block

Experimental

Celiac Block with triamcinolone and bupivicaine Intra Plexus Triamcinolone and Bupivicaine Injection

干预措施: Intra Plexus Triamcinolone and Bupivicaine Injection (Drug)

EUS without Celiac Block

Active Comparator

Patients will undergo EUS but no celiac block will be performed

干预措施: No Celiac Block (Procedure)

结局指标

主要结局

Long Term CHANGE in Pain Scores

时间窗: 24 weeks

Primary outcomes will be the CHANGE pain score (as assessed by the visual-analogue-scale and M-ANNHEIM score assessed between time 0 and 24 weeks post procedure in those who undergo EUS without block (control) compared to those who undergo EUS with block

次要结局

  • Hospital re-admission(24 weeks)
  • CHANGE Pain medication requirements(24 weeks)
  • Procedure Complications(2 weeks)

研究者

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

James Buxbaum

Assistant Professor

University of Southern California

研究点 (1)

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