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临床试验/NCT00805805
NCT00805805已完成3 期

Phase III Trial of Tetrathiomolybdate (TM) in Primary Biliary Cirrhosis

George Brewer1 个研究点 分布在 1 个国家目标入组 29 人开始时间: 2006年4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
George Brewer
入组人数
29
试验地点
1
主要终点
Improvement in drug treated group vs placebo group in two liver function tests and one serum cytokine measurement

研究概览

简要总结

The University of Michigan is conducting a study investigating a potential new treatment aimed at slowing/halting progression of primary biliary cirrhosis. This will be a 2 arm double blind study in which half of the patients will be randomly selected to receive a placebo (capsule with no active ingredient) and half will receive the new treatment drug, tetrathiomolybdate. Neither the patient nor the treating physician will know which arm the patient is in. The length of the study for each patient is 24 months of drug therapy. Lab draws will be necessary weekly for the first 6 weeks of the study, followed by every other week for 3 weeks, and then monthly for the remainder of the 2 year period. In addition, intermittent history and physicals and urine samples will also be necessary. There is no cost to you for any experimental treatment. All patients in both arms will continue on ursodiol and receive standard of care treatment

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
Quadruple (Participant, Care Provider, Investigator, 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

  • Generally medically healthy
  • Age 18 and older
  • Documented primary biliary cirrhosis
  • Alkaline phosphatase > 137

排除标准

  • Severe liver decompensation
  • Requirement for renal dialysis
  • Pregnancy or nursing
  • Meld score > 15 (13-15 will require a physician's clinical judgment)
  • Uncontrolled congestive heart failure
  • Severe diabetic neuropathy
  • Severe pulmonary disease
  • Advanced cancer
  • Requirement for steroid therapy
  • Uncontrolled ascites, variceal hemorrhage or spontaneous bacterial peritonitis
  • Pregnant or nursing

研究组 & 干预措施

1

Experimental

Tetrathiomolybdate with ursodiol

干预措施: Tetrathiomolybdate (Drug)

2

Placebo Comparator

Placebo with ursodiol

干预措施: Placebo (Other)

结局指标

主要结局

Improvement in drug treated group vs placebo group in two liver function tests and one serum cytokine measurement

时间窗: 2 years

次要结局

  • Improvement in drug treated group vs placebo group in serum CRP or interleukin-1-beta-levels(2 years)

研究者

发起方
George Brewer
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

George Brewer

Professor

University of Michigan

研究点 (1)

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