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临床试验/NCT00806611
NCT00806611已完成3 期

A Randomized, Controlled Trial of Intraoperative Celiac Plexus Neurolysis for Patients With Operable (Resectable and Unresectable) Pancreatic and Periampullary Cancer

Sidney Kimmel Cancer Center at Thomas Jefferson University1 个研究点 分布在 1 个国家目标入组 438 人开始时间: 2008年9月最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
438
试验地点
1
主要终点
The primary endpoint is cancer related pain control.

研究概览

简要总结

Determine if the addition of an intraoperative ethanol celiac plexus neurolysis (alcohol block) in patients undergoing surgical intervention for pancreatic cancer will result in a decrease in cancer associated pain

详细描述

Pancreatic adenocarcinoma is the fourth leading cause of cancer related death in the United States and is usually fatal. Surgery provides the only chance for long-term survival. Pain is a significant, often difficult to control component of survivorship for many who succumb to this disease. The purpose of this trial is to evaluate the effect of ethanol celiac plexus neurolysis (alcohol nerve block) in patients undergoing surgical intervention for pancreatic cancer. Patients undergoing surgery for pancreatic cancer will be enrolled in a prospective randomized double blind placebo controlled clinical trial.

This protocol is designed to definitively determine the role of ethanol celiac plexus neurolysis as a simple addition to the surgical management of pancreatic adenocarcinoma and help define the standard of care for cancer associated pain management in this disease.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Investigator)

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

  • Preoperative imaging indicates possibility of resectable pancreatic cancer
  • Intraoperative biopsy histologically confirming pancreatic adenocarcinoma

排除标准

  • 未提供

研究组 & 干预措施

50% Ethanol

Experimental

Operating surgeon injects 20 ml of 50% ethanol on each side of the aorta at the level of the celiac axis with a 20 or 22 gauge spinal needle

干预措施: Alcohol Block (Procedure)

Placebo

Placebo Comparator

Operating surgeon injects 20 ml of saline on each side of the aorta at the level of the celiac axis with a 20 or 22 gauge spinal needle

干预措施: Alcohol Block (Procedure)

结局指标

主要结局

The primary endpoint is cancer related pain control.

时间窗: Increased pain at 12 months in subjects with resectable tumors; increased pain at 3 months in subjects with unresectable tumors

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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