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临床试验/NCT03221764
NCT03221764已完成2 期

The Intra-Operative Application of Amiodarone Releasing Hydrogel to Prevent Postoperative Atrial Fibrillation in Patients Undergoing Lung Transplantation

University of Louisville1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2017年10月19日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
20
试验地点
1
主要终点
Post Operative Atrial Fibrillation

研究概览

简要总结

This study will prospectively evaluate the use of an amiodarone releasing hydrogel applied to the pulmonary veins and atria at the time of lung transplantation. This study will include patients undergoing lung transplantation at Jewish Hospital, Louisville KY. The prospective group will be compared to historical controls from the same institution. Investigators will access medical records and database entries for those patients undergoing lung transplantation after January 1st 2005 in order to obtain matched controls for analysis. Informed consent will be obtained from the prospective cohort prior to patient enrollment. This pilot study will be used to obtain preliminary data in order to proceed with a larger randomized control trial.

详细描述

Approximately 1900 transplants are performed in the US annually. Lung transplantation remains the gold standard treatment for patients with end stage lung disease. This includes patients with range of etiologies such as Idiopathic Pulmonary Fibrosis, COPD and Cystic Fibrosis. One of the more common post-operative complications in patients undergoing lung transplantation is the development of atrial fibrillation. Recent studies have demonstrated that approximately 1/3 of patients will develop atrial fibrillation during their post-operative course. While it is uncertain if the development of post-operative atrial fibrillation affects survival, it does significantly increase length of hospital stay. Importantly, a portion of the patients that develop atrial fibrillation post-operatively will require cardioversion prior to discharge.

Currently one of the main stays of treatment for post-operative atrial fibrillation is systemic (oral or intravenous) amiodarone, which is a class III antiarrhythmic agent. While this particular drug is effective, it does carry the risk of several known complications. Due to the drug's pharmacokinetics, amiodarone concentrates in organs with high lipid content such as the thyroid, liver and lung. Amiodarone has several known adverse effects on the lung ranging from acute respiratory distress syndrome to more chronic disease such as Interstitial pulmonary fibrosis. Amiodarone can have detrimental effects on the liver which in rare cases could lead to cirrhosis. Additionally, amiodarone can cause thyrotoxicosis as early as a few weeks after the initiation of amiodarone.

The adverse events listed above are related to the cumulative dose of amiodarone. Typically, when amiodarone is initiated, patients receive a loading dose of 600-800mg daily until the cumulative dose reaches 10 grams, after which patients will receive 200mg daily as a maintenance dose. Minimizing the cumulative dose of amiodarone by using a local application, could mitigate the potential adverse drug toxicities. In a previous study, the application of an amiodarone releasing hydrogel performed intraoperatively was shown to significantly decrease the rates of post-operative atrial fibrillation in patients undergoing coronary artery bypass. Currently for patients undergoing lung transplantation, there is not a safe and effective measure available to prevent post-operative atrial fibrillation.

The Investigators aim to study the intraoperative application of an amiodarone containing hydrogel for prevention of post-operative atrial fibrillation in lung transplant patients.

In patients undergoing lung transplantation, post-operative atrial fibrillation is common and leads to prolonged hospital course and increased healthcare expenditures. Amiodarone is a main stay of therapy for atrial fibrillation, however this drug does have potential serious complications when administered systemically. The local application of amiodarone, could potentially decrease the rates of atrial fibrillation, while avoiding the systemic complications. This has the potential to decrease length of stay and decrease additional procedures (ie. Cardioversion) in patients undergoing lung transplantation.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subject or legal representative has signed Informed Consent Form (ICF)
  • Undergoing lung transplant at the Jewish Hospital
  • Age ≥ 18 years
  • Subjects willing and able to comply with the follow up requirements of the study

排除标准

  • Patients with previous history of atrial fibrillation.
  • Patients with previously documented allergy or adverse reaction to amiodarone.
  • Patients with previous ablation for atrial fibrillation
  • Patients with an implantable pacemaker.

研究组 & 干预措施

Amiodarone with CoSeal administered with CO2 driver

Experimental

Lung Transplant Recipients who receive Intraoperative application of an Amiodarone containing hydrogel at the time of transplant.

干预措施: Amiodarone with CoSeal (Drug)

Amiodarone with CoSeal administered with CO2 driver

Experimental

Lung Transplant Recipients who receive Intraoperative application of an Amiodarone containing hydrogel at the time of transplant.

干预措施: CO2 driver (Device)

结局指标

主要结局

Post Operative Atrial Fibrillation

时间窗: Patients will be monitored for up to one year following lung transplant

Patient that developed atrial fibrillation after undergoing lung transplantation

次要结局

  • Atrial Fibrillation Requiring Intervention(From transplant to discharge from hospital, up to 1 year)
  • Anti-Arrhythmic Medication at Discharge(1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Victor Van Berkel

Assistant Professor

University of Louisville

研究点 (1)

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