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临床试验/NCT00322868
NCT00322868已完成不适用

A Pilot Study Assessing the Safety and Efficacy of Pioglitazone as an Anti-inflammatory Agent for the Treatment of CF Lung Disease in Patients With Cystic Fibrosis

University Hospitals Cleveland Medical Center1 个研究点 分布在 1 个国家目标入组 21 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
不适用
状态
已完成
入组人数
21
试验地点
1
主要终点
Sputum TNFα

研究概览

简要总结

Study Hypothesis: Pioglitazone may decrease inflammation in cystic fibrosis lung disease.

Primary outcomes: Markers of inflammation (neutrophils, elastase, cytokines and bacteria)will be measured in induced sputum specimens before and after a 4 week treatment period with pioglitazone in clinically stable CF patients.

详细描述

  • Single-center, open label study of pioglitazone in clinically stable patients with mild to moderate CF lung disease
  • Induced sputum will be obtained from each subject at enrollment (Baseline) and again following 28 days of pioglitazone treatment (End of Treatment)
  • Changes in markers of inflammation in the sputum samples will be assessed
  • Safety measures, including complete blood count (CBC), serum chemistry, Erythrocyte sedimentation rate (ESR), C-Reactive Protein (CRP), urinalysis and spirometry, will also be assessed

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

盲法说明

This was open-label and no one was masked.

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

  • Male or female >= 28 years of age
  • Confirmed diagnosis of cystic fibrosis
  • Forced Expiratory Volume in 1 second (FEV1) >= 40% predicted
  • Clinically stable
  • Ability to reproduce spirometry
  • Ability to understand and sign the informed consent

排除标准

  • Use of an investigational agent within 4-week period prior to Visit 1
  • Chronic daily use of ibuprofen or other NSAIDS
  • Chronic daily use of insulin,oral diabetic agents or oral hypoglycemic agents
  • History of hypersensitivity to beta agonists
  • History of hypersensitivity to glitazones
  • Oxygen saturation<92%
  • Pregnant, breastfeeding or unwilling to practice acceptable birth control
  • History of hemoptysis >30cc per episode within 30 days prior to Visit 1
  • Significant history of hepatic, cardiovascular, renal,neurologic, hematologic or peptic ulcer disease
  • Serum Glutamic-Oxaloacetic Transaminase (SGOT)/(Serum Glutamic Pyruvic Transaminase (SGPT) >3 times the upper limit of normal at screening, documented biliary cirrhosis,or portal hypertension
  • Creatinine > 1.8 mg/dL at screening
  • Inability to swallow pills
  • Presence or abnormality that in the opinion of the investigator would compromise the safety or the quality of the data
  • Subjects who have routinely taken ibuprofen or other NSAIDS; prednisone or other systemic corticosteroids, or insulin, or oral diabetic agents within 4 weeks prior to visit 1 or who have taken these medications as needed within 72 hours prior to visit one will be excluded

研究组 & 干预措施

Pioglitazone

Experimental

All subjects treated for 28 days with pioglitazone, 30 mg orally, once daily Other names: Actos, Takeda

干预措施: pioglitazone (Drug)

结局指标

主要结局

Sputum TNFα

时间窗: Day 0 and Day 29

The concentration of Tumor Necrosis Factor-α (TNFα) log 10 (pg/mL)

Sputum Neutrophil Count

时间窗: Day 0 and Day 29

sputum neutrophils log 10 (cells/mL)

Sputum White Cell Count

时间窗: Day 0 and Day 29

The total number of white cells log 10 cells/mL

Sputum Neutrophil Percent

时间窗: Day 0 and Day 29

Neutrophils as a percent of the total white cells.

Sputum Active Elastase

时间窗: Day 0 and Day 29

Log 10 of Concentration of active Elastase in mcg/mL

Sputum IL-8

时间窗: Day 0 and Day 29

Concentration of Interleukin-8 log 10 (pg/mL)

Sputum IL-1ß

时间窗: Day 0 and Day 29

The concentration of Interleukin-1ß (IL-1ß) log 10 (pg/mL)

Sputum IL-6

时间窗: Day 0 and Day 29

The concentration of Interleukin-6 (IL-6) log 10 (pg/mL)

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

Michael W. Konstan

Professor of Pediatrics

University Hospitals Cleveland Medical Center

研究点 (1)

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