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临床试验/NCT00116402
NCT00116402已完成1 期

A Pilot Study of the Mechanism of Synergism Between Fluticasone (FP) and Salmeterol in Preventing Chronic Obstructive Pulmonary Disease (COPD) Exacerbations

University of Chicago1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2005年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
15
试验地点
1
主要终点
To evaluate blood and airway neutrophil population in COPD patients by examining adhesion and migration in patients with mild to moderate COPD

研究概览

简要总结

The purpose of this study is to evaluate the blood and airway of subjects with mild to moderate COPD while undergoing standard treatment.

详细描述

Our objective is to examine the mechanism of the additive/synergistic properties of b2-adrenoceptor stimulation and corticosteroid receptor activation in:

  • Preventing neutrophil adhesion to specific endothelial ligands, e.g. ICAM-1 and
  • Undergoing activation as a consequence of this adhesion.

We hypothesize that combination therapy with salmeterol + fluticasone (FP) will:

  • Augment the inhibition of adhesion of neutrophils obtained from the peripheral blood of study subjects in vitro, by blocking gIV-PLA2 translocation to the nuclear membrane as for eosinophils;
  • Augment the inhibition of transendothelial migration of neutrophils into airways of subjects with chronic obstructive pulmonary disease;
  • Augment the numbers and concentrations of pro-inflammatory products in the bronchoalveolar lavage fluid; and
  • Decrease the number of neutrophils in the bronchial tissue of endobronchial biopsies of treated patients.

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
None

入排标准

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

入选标准

  • Males or females > 50 years of age
  • Physiologic evidence of COPD defined per ATS guidelines as: cigarette smoking history >20 pack years, FEV1/FVC <70%
  • Patients must have a post-bronchodilator FEV1 >50% of predicted value at enrollment
  • Patient must have an O2 saturation measure by pulse oximetry >90% on RA
  • Must be able to participate in the study, willing to give informed consent, and comply with the study restrictions

排除标准

  • Women of child-bearing potential defined as females who are less than 5 years post menopausal unless they have had a hysterectomy or bilateral oophorectomy
  • Observation of any solitary nodule in the lung requiring further medical intervention
  • Patients on maintenance therapy with oral steroids
  • Patients with giant bullous disease
  • Significant other medical conditions, which in the opinion of the investigator, will interfere with the patient's ability to perform the study tests
  • Presence of a coagulopathy as defined by a platelet count <100,000/mm3, and PT and PTT >1.2 x the upper limit of normal
  • Concurrent enrollment or participation in any other clinical trials within the past 30 days
  • Primary diagnosis of asthma
  • History of alpha 1 antitrypsin deficiency
  • Any clinically significant and active pulmonary disease that could contribute to dyspnea
  • Current systemic and inhaled steroids and theophylline

研究组 & 干预措施

1

Active Comparator

will start with fluticasone 220 mcg BID first and then crossover to combination therapy with salmeterol 50 mcg BID

干预措施: fluticasone and salmeterol (Drug)

2

Active Comparator

salmeterol 50 mcg BID then crossover to combination therapy with fluticasone 220 mcg BID

干预措施: fluticasone and salmeterol (Drug)

结局指标

主要结局

To evaluate blood and airway neutrophil population in COPD patients by examining adhesion and migration in patients with mild to moderate COPD

时间窗: 12 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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