Safety and Efficacy of Pioglitazone as an Anti-inflammatory for the Treatment of Cystic Fibrosis (CF) Lung Disease
2018年2月21日 更新者:Michael W. Konstan、University Hospitals Cleveland Medical Center
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
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.
研究概览
详细说明
- 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
研究类型
介入性
注册 (实际的)
21
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
Ohio
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Cleveland、Ohio、美国、44106
- Rainbow Babies and Children's Hospital
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-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 及以上 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Pioglitazone
All subjects treated for 28 days with pioglitazone, 30 mg orally, once daily Other names: Actos, Takeda
|
All subjects treated for 28 days with pioglitazone, 30 mg orally, once daily.
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Sputum White Cell Count
大体时间:Day 0 and Day 29
|
The total number of white cells log 10 cells/mL
|
Day 0 and Day 29
|
|
Sputum Neutrophil Count
大体时间:Day 0 and Day 29
|
sputum neutrophils log 10 (cells/mL)
|
Day 0 and Day 29
|
|
Sputum Neutrophil Percent
大体时间:Day 0 and Day 29
|
Neutrophils as a percent of the total white cells.
|
Day 0 and Day 29
|
|
Sputum Active Elastase
大体时间:Day 0 and Day 29
|
Log 10 of Concentration of active Elastase in mcg/mL
|
Day 0 and Day 29
|
|
Sputum TNFα
大体时间:Day 0 and Day 29
|
The concentration of Tumor Necrosis Factor-α (TNFα) log 10 (pg/mL)
|
Day 0 and Day 29
|
|
Sputum IL-1ß
大体时间:Day 0 and Day 29
|
The concentration of Interleukin-1ß (IL-1ß) log 10 (pg/mL)
|
Day 0 and Day 29
|
|
Sputum IL-6
大体时间:Day 0 and Day 29
|
The concentration of Interleukin-6 (IL-6) log 10 (pg/mL)
|
Day 0 and Day 29
|
|
Sputum IL-8
大体时间:Day 0 and Day 29
|
Concentration of Interleukin-8 log 10 (pg/mL)
|
Day 0 and Day 29
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Michael W. Konstan, MD、Case University and Rainbow Babies and Children's Hospital
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2006年4月1日
初级完成 (实际的)
2006年12月1日
研究完成 (实际的)
2007年4月1日
研究注册日期
首次提交
2006年5月4日
首先提交符合 QC 标准的
2006年5月4日
首次发布 (估计)
2006年5月8日
研究记录更新
最后更新发布 (实际的)
2018年2月23日
上次提交的符合 QC 标准的更新
2018年2月21日
最后验证
2018年2月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.