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临床试验/NCT00304356
NCT00304356已完成3 期

Compassionate Use of Nitazoxanide for the Treatment of Clostridium Difficile Colitis in Patients Who Have Failed Conventional Therapy

Daniel M. Musher MD2 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2004年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
22
试验地点
2
主要终点
Nitazoxanide

研究概览

简要总结

The purpose of this study is for compassionate use of nitazoxanide in the treatment of diarrheal disease due to Clostridium difficile infection when the patient has failed previous treatment with metronidazole or vancomycin.

详细描述

Clostridium difficile is the leading cause of nosocomial diarrheal disease associated with antibiotic therapy. This is a debilitating condition with substantial morbidity and a mortality that may be around 2-3%. There has been an enormous increase in this disease at the VA Medical Center during the past two years, just as has occurred at other hospitals throughout the United States.

Currently recommended therapy for this condition is metronidazole, given orally. About 15-20% of patients fail to respond to initial therapy with metronidazole, and another 20% relapse after treatment. Relapses may be treated with another course of metronidazole; about one-half will respond to this therapy. The failures are treated with oral vancomycin, but this drug also has a failure rate of 10-20%. There is, at present, no other accepted therapy (although some articles in the literature favor vancomycin with ingested bacteria from benign species). Furthermore, there is a strong risk to the emergence of resistant bacteria when hospitalized patients are treated with oral vancomycin.

Nitazoxanide is an FDA approved drug that is marketed in the U.S. and has been widely used throughout the world to treat parasitic diseases of the gastrointestinal tract; several million children have been treated with this drug during the past decade. Nitazoxanide has been approved as an antiprotozoal agent for oral administration in pediatric patients, ages 1 through 11, with diarrhea. The drug acts by interfering with anaerobic metabolic pathways, and it has been shown to have excellent in vitro activity against C. difficile. We hypothesized that this drug was both safe and effective as an alternative in patients who have diarrheal disease caused by C. difficile. The IRB approved a double-blind protocol to compare metronidazole with nitazoxanide, and we have treated a total of 16 patients so far under this protocol.

In our IRB-approved double blind study (by design, two thirds of the subjects have been randomized to the nitazoxanide), our patients have appeared to have a good response rate -- so good, in fact, that we think that nitazoxanide may be a better drug to treat this infection than either metronidazole or vancomycin.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

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

  • Patient must be > 18 years of age
  • Clinical diagnosis of C. difficile associated disease, based on the new onset of diarrhea, abdominal discomfort, or otherwise unexplained fever or leukocytosis
  • Diagnosis of C. difficile colitis proven by positive assay for C. difficile toxin in feces
  • Disease has been treated, and the symptoms failed to respond to treatment with metronidazole or vancomycin, or symptoms promptly relapsed after completing a course of therapy with either of these drugs
  • Able to take oral medication

排除标准

  • Patients with other recognized causes of diarrhea or colitis
  • Women of child bearing age who are pregnant, breast feeding, or not using birth control
  • Patients taking coumadin, phenytoin, celecoxib, or losartan
  • Patients with renal insufficiency (BUN or creatinine >2 times baseline)
  • Serious systemic disorder incompatible with the study

研究组 & 干预措施

active drug

Other

500 mg nitazoxanide bid given to patient

干预措施: Nitazoxanide (Drug)

结局指标

主要结局

Nitazoxanide

时间窗: 30 days

stopping of diarrhea

次要结局

未报告次要终点

研究者

发起方
Daniel M. Musher MD
申办方类型
Fed
责任方
Sponsor Investigator
主要研究者

Daniel M. Musher MD

PI

Michael E. DeBakey VA Medical Center

研究点 (2)

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