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临床试验/NCT00432835
NCT00432835已完成3 期

Double-Blind Placebo-Controlled Cross-Over Design With Wash-Out for Temporary Gastric Electrical Stimulation for Drug Refractory Gastroparesis

University of Mississippi Medical Center2 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2005年8月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
58
试验地点
2
主要终点
Symptom of Vomiting Associated With Gastroparesis

研究概览

简要总结

The purpose of this research is to determine if temporary gastric electrical stimulation will help improve symptoms of gastroparesis (abnormal stomach emptying). We hypothesize that when the device is ON, Gastrointestinal symptoms will decrease by at least 50% from baseline.

详细描述

Gastric Electrical Stimulation is an established treatment for drug-refractory patients who have the symptoms of gastroparesis/gastropathy. The symptoms of GP are nausea, vomiting, anorexia/early satiety, bloating/distention and abdominal pain and are classically associated with delayed gastric emptying of solids. The technique of GES was first used, in a patient seen at University of Tennesse-Memphis in 1993 and has undergone several clinical trials, particularly the GEMS trial, a feasibility trial starting in 1995 and the WAVESS trial, a double-blind trial begun in 1997. Both were international trials, showing promising results, and both have been published in the last 2 years. However, a number of issues related to who would benefit the most from Gastric Electrical Stimulation therapy have emerged. Among these issues are whether patients with etiologies other than diabetic or idiopathic gastroparesis, such as post-surgical gastropathy, which is often related to rapid, not delayed gastric emptying could be helped.

Most recently a technique for the temporary placement of a Gastric Electrical Stimulation electrode in the stomach with an upper endoscope, combined with an external Gastric Electrical Stimulation device, has been tried and validated, first at UAMS in Little Rock, AR, beginning in 2001 and more recently here at UMMC, beginning later in 2001 and up until the present time. Using the technique of temporary gastric electrical stimulation, we have been able to demonstrate that TempStim can quickly demonstrate (in a manner of days) that a patient will respond to temporary GES, as quantified by a decrease in GI total symptoms and an improvement and normalization in solid gastric emptying.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Sex: Male of Female
  • Age Range: 18 to 70 inclusive
  • Patients with GP of diabetic, surgically related or idiopathic etiology.
  • Symptoms of GP for >/= 1 year.
  • Refractory or intolerant to antiemetic drug classes (antihistamines and phenothiazines, serotonin receptor antagonists, dopamine receptor antagonists)
  • Chronic vomiting and/or nausea with 7 or more episodes per week for either symptom irrespective of GET values.
  • The patient is willing and able to provide informed consent.
  • The patient is willing and able to return for required follow-up visits.

排除标准

  • Patients < 18 or >70 years in age.
  • Patients with an active infection of any kind.
  • Patients who the investigator determines are not candidates for endoscopic procedures.
  • Women who are pregnant
  • Inability or unwillingness to provide informed consent
  • Unwilling or unable to return for required follow-up visits and examinations.
  • Patients who are currently enrolled in another investigation of a medical device or drug.

结局指标

主要结局

Symptom of Vomiting Associated With Gastroparesis

时间窗: Study Day 0 (Baseline), Day 3, Day 7

Likert Scale 0-4 (low-high) using a patient reported outcomes tool

Symptom of Nausea Associated With Gastroparesis

时间窗: Study Day 0 (Baseline), Day 3, Day 7

Likert Scale 0-4 (low-high) using a patient reported outcomes tool

Symptom of Gastric Emptying Time (GET) Associated With Gastroparesis

时间窗: Study Day 0 (Baseline), Day 4, Day 8

Transit time of a radio-labeled meal through the stomach, measured by scintigraphy for %contents remaining in the stomach at 1 hour, 2 hours, and 4 hours. GET measures were obtained at baseline, during the period allowed for 'washout', and on the final study day.

次要结局

未报告次要终点

研究者

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

Thomas Abell, MD

Principal Investigator, Professor of Medicine, Director, Division of Digestive Diseases

University of Mississippi Medical Center

研究点 (2)

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