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临床试验/NCT02220634
NCT02220634终止不适用

Regadenoson for Acute Vasoreactivity Testing in Pulmonary Hypertension

National Jewish Health1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2014年8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
终止
入组人数
10
试验地点
1
主要终点
Number of people

研究概览

简要总结

The purpose of this study is to see if Regadenoson may offer improved ease of use, single dose administration, and better tolerance for testing for pulmonary hypertension than iNO. You will be screened to make sure Regadenoson is safe for you with a clinical evaluation, blood tests, and an ECG.

详细描述

Pulmonary hypertension (PH) is an increase of blood pressure in the pulmonary vascular system that could cause shortness of breath, dizziness, leg swelling and heart failure. .

The diagnosis of PH requires confirmation of elevated pulmonary pressures.. Right heart catheterization (RHC) is a procedure to determine the diagnosis of PH. .

This research study is looking at the effect of intravenous infusion of the medication Regadenoson on pulmonary vasodilator response compared to the inhaled nitric oxide (iNO) response. iNO is the current standard of care practice.

The purpose of this study is to see if Regadenoson may offer improved ease of use, single dose administration, and better tolerance for testing for pulmonary hypertension than iNO. You will be screened to make sure Regadenoson is safe for you with a clinical evaluation, blood tests, and an ECG.

You will be asked to sign this informed consent form. Then, you will undergo right heart catheterization as part of your clinical care. Those who are positive for pulmonary hypertension will then undergo Regadenoson infusion and a inhaled iNO. Prior to the infusion, subjects will be asked if they have had in the last 12 hours any caffeine-containing foods or beverages, caffeine-containing medications such as theophylline 12 hours prior. Vital sign measurements will be taken to measure your heart. For those subjects that have low heart volume they will be given 500 cc of normal saline in their IV. Vital sign measurements will be taken again to make sure your heart volume is in the normal range. The doctor will administer Regadenoson 0.4 mg intravenously and this will cause your heart rate to increase. The doctor will be taking heart measurements 90 seconds, 5 minutes, 10 minutes, and 20 minutes after administration. Approximately 30 minutes after the Regadenoson has been administered you will be given iNO by facemask for 5 minutes.

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

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-75 years old
  • Diagnosis of RHC-proven PH
  • Mean pulmonary artery pressure (mPAP) > 25 mmHg
  • Pulmonary vascular resistance (PVR) > 3 woods units
  • Pulmonary capillary wedge pressure (PCWP) < 15 mmHg).

排除标准

  • Second- or third-degree AV block or sinus node dysfunction
  • Known hypersensitivity to adenosine or regadenoson
  • Systolic blood pressure < 90mm Hg
  • Active bronchospasm
  • Autonomic dysfunction as defined by prior diagnosis of:
  • Postural Orthostatic Tachycardia Syndrome (POTS)
  • Neurocardiogenic Syncope (NCS)
  • Neurally Mediated Hypotension (NMH)
  • Vasovagal Syncope
  • Hypovolemia
  • > 40% Left main coronary stenosis
  • Moderate or > valvular stenosis
  • Pericarditis/pericardial effusions
  • > 70% carotid artery stenosis
  • Positive urine pregnancy test

研究组 & 干预措施

Regadenoson

Experimental

Intravenous infusion of the A2A agonist regadenoson has a preferential vasodilator effect on pulmonary vasculature that is comparable to iNO, the current gold standard for pulmonary vasoreactivity studies.

干预措施: Regadenoson (Drug)

结局指标

主要结局

Number of people

时间窗: 5 years

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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