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临床试验/NCT00701207
NCT00701207已完成早期 1 期

Modulation of Pulmonary Sarcoidosis by Nicotinic Acetylcholine Receptors

Elliott Crouser MD1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2008年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
发起方
入组人数
64
试验地点
1
主要终点
To determine if nicotine treatment reduces lung inflammation.

研究概览

简要总结

The purpose of this study is to compare peoples with disease (sarcoidosis) to those without disease. We want to see if people with sarcoidosis have a different immune response to those people without disease.

The goal of this study is to see if the nicotine patch is an anti-inflammatory treatment for sarcoidosis.

详细描述

Until recently, there was no good explanation for the fact that smoking cigarettes actually reduces the risk of sarcoidosis. Research studies have shown that the nicotine, a common component of cigarette smoke, strongly suppresses the immune system and reduces the type of inflammation that is characteristic of sarcoidosis in the lungs. We propose that nicotine treatment, administered in the form of a skin patch, will reduce the severity of lung disease in patients with sarcoidosis. Sarcoidosis patients who volunteer to participate in this study will submit standardized questionnaires relating to their quality of life and the severity of their shortness of breath before and after treatment. We will also compare objective measures of lung function, radiographic parameters, and the severity of lung inflammation. We predict that nicotine treatment will reduce the severity of sarcoidosis symptoms, improve lung function, and resolve lung inflammation. If our hypothesis is proven to be correct in this relatively small group of patients, we will perform additional studies in a larger group of patients and will consider the features of sarcoidosis patients that predict a favorable response to nicotine and other nicotine-like drugs. If nicotine is ultimately found to be an effective treatment for sarcoidosis, it may replace some of the existing treatments which are frequently ineffective and have unacceptable side-effects.

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
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

  • • Symptomatic (active) granulomatous lung disease (radiographic stage II or III disease) at least 6 months after the diagnosis. This selects patients that have the chronically active variant of sarcoidosis and will likely require long-term treatment (33).

排除标准

  • • Active smokers,
  • Previous splenectomy,
  • Those requiring high-dose immunosuppression [i.e., ≥ 0.2 mg/kg/day prednisone (or equivalent) or > 10 mg/week methotrexate or requires second line cytolytic agents (e.g., cyclophosphamide, azathioprine) or anti-TNF treatments (e.g., thalidomide, anti-TNF antibodies, etc.)] to control disease activity.
  • We will also exclude patients at high risk of complications relating to the use of nicotine. This will include patients with a known intolerance of nicotine or those with active cardiac or central nervous system disease who are at higher risk of cardiac arrhythmias or seizures.
  • We will also exclude patients with extensive pulmonary fibrosis based upon lung biopsy or high resolution CT scan criterion

研究组 & 干预措施

1.

Experimental

nicotine patch; transdermal patch 7mg, 14 mg., 21 mg. 3 months

干预措施: nicotine patch (Drug)

结局指标

主要结局

To determine if nicotine treatment reduces lung inflammation.

时间窗: 3 months

Normalization of immune response

次要结局

  • To determine if expression of α7 nAChR on monocytes/macrophages derived from the blood/lungs correlates with the severity of pulmonary sarcoidosis.(3 months)

研究者

发起方
Elliott Crouser MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Elliott Crouser MD

Medical Director, Intensive Care Unit, UHE

Ohio State University

研究点 (1)

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