Hospital-Based Program for Treatment of Severe Cardiopulmonary Disease With Inhaled Nitric Oxide
2016年9月8日 更新者：Mallinckrodt
Development of a Hospital-Based Home Program for the Use of Inhaled Nitric Oxide in the Chronic Management of Severe Cardiopulmonary Diseases
The purpose of this program is to evaluate the logistic issues and patient requirements for chronic pulsed INOmax delivery in ambulatory, home-care patients.
To understand patient needs, patients with a variety of underlying diseases will be included.
Safety of chronic therapy will be monitored by serial measurements of methemoglobin, platelet function assay and reported adverse events.
研究概览
详细说明
This study will help develop a comprehensive home care program using INOmax delivery systems. This study will enroll a limited number of patients (5-7) from several disease categories in order to develop the experience with testing acute and chronic responsiveness to INO therapy. The following groups will be tested:
- Primary pulmonary hypertension (PPH)
- Severe pulmonary hypertension due to congenital (anatomic) heart disease
- Pulmonary hypertension or severe impairment of gas exchange in infants and children with chronic lung disease
- Pulmonary hypertension or severe impairment of gas exchange due to severe chronic lung disease in adults
- Pulmonary hypertension or severe impairment of gas exchange in hematologic and transplant disorders - young children and adults with sickle cell disease, chronic lung disease after bone marrow transplant, cardiac transplant, or lung transplant
研究类型
介入性
注册 (实际的)
7
阶段
- 阶段2
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
-
-
Colorado
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Denver、Colorado、美国、80262
- University Of Colorado Hospital
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Denver、Colorado、美国、80262
- The Children's Hospital
-
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Rhode Island
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Providence、Rhode Island、美国、02903
- Rhode Island Hospital
-
-
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
5年 及以上 (孩子、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:
- Patients with pulmonary arterial hypertension (PAH) as defines by a mean pulmonary artery pressure (PAP) of 25 mmHg or greater by cardiac catheterization within the previous 12 months AND/OR Patients with chronic lung disease with severe impairment of gas exchange unresponsive to conventional medical management.
- If patient is receiving prostacyclin infusion treatment it must have been started at least one month prior to starting INO therapy. Patients will not be withdrawn from the study if started on other medications for treatment of pulmonary hypertension.
- Ability to establish a clinical investigator and a drug shipment site in the local area.
Exclusion Criteria:
- The Principal Investigator has determined that the patient and/or caregiver is/are unable to manage safe administration of home nitric oxide therapy and maintain appropriate drug accountability and storage.
- Women who are pregnant or nursing.
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：非随机化
- 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：1
Inhaled Nitric Oxide will be delivered through the INOpulse® at a Low Dose Range (3mL to 10mL; in 1mL increments) and Ultra Low Dose Ranges (0.5mL to 4mL; 0.5mL, then 1 to 4mL in 1mL increments).
|
Inhaled Nitric Oxide will be delivered through the INOpulse® at a Low Dose Range (3mL to 10mL; in 1mL increments) and Ultra Low Dose Ranges (0.5mL to 4mL; 0.5mL, then 1 to 4mL in 1mL increments).
其他名称：
|
研究衡量的是什么？
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Methemoglobin level
大体时间：24 and 72 hours after treatment start, then at 1, 3, 6, 9 and 12 months
|
24 and 72 hours after treatment start, then at 1, 3, 6, 9 and 12 months
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Vital Signs
大体时间：taken at 1, 2, 3, 4, 24, and 72 hours after treatment begins, then at 1, 3, 6, 9 and 12 months
|
taken at 1, 2, 3, 4, 24, and 72 hours after treatment begins, then at 1, 3, 6, 9 and 12 months
|
|
Pulse Oximetry
大体时间：taken at 1, 2, 3, 4, 24, and 72 hours after treatment start and then at 1, 3, 6, 9 and 12 months
|
taken at 1, 2, 3, 4, 24, and 72 hours after treatment start and then at 1, 3, 6, 9 and 12 months
|
|
Adverse Event Occurence
大体时间：Study Duration
|
Study Duration
|
|
Echocardiogram
大体时间：At 72 hours after treatment start, then at 3, 6, 9 and 12 months
|
At 72 hours after treatment start, then at 3, 6, 9 and 12 months
|
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。
赞助
调查人员
- 首席研究员：Steven H Abman, MD、Children's Hospital Colorado
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
2002年4月1日
初级完成 (实际的)
2005年12月1日
研究完成 (实际的)
2005年12月1日
研究注册日期
首次提交
2002年7月10日
首先提交符合 QC 标准的
2002年7月10日
首次发布 (估计)
2002年7月11日
研究记录更新
最后更新发布 (估计)
2016年9月9日
上次提交的符合 QC 标准的更新
2016年9月8日
最后验证
2016年9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.