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临床试验/NCT01254708
NCT01254708暂停2 期

A Pilot Study to Determine the Safety and Clinical Efficacy of Once-Weekly Inhaled AmBisome for the Prevention of Aspergillus Colonization in Lung Transplant Recipients

University Health Network, Toronto1 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2012年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
暂停
入组人数
4
试验地点
1
主要终点
Pulmonary Function

研究概览

简要总结

Lung transplant recipients have the highest rate of Invasive Aspergillus (IA)infection among solid organ transplant recipients. The most important risk factor for the development of IA (which is associated with disease and death) is colonization of the organism in the respiratory tract.

Azoles are used to prevent the development of IA. Puffers containing antifungal medication can be used to treat the lungs without the need to worry about the medication interactions & side-effects in the blood. An example of this is the aerosolized amphotericin B. Its use is limited by the patients' tolerating this medication that may cause cough, nausea & contraction of the air pathways.

The lipid preparation is better tolerated and has longer dosing interval than inhaled amphotericin B. The investigators propose a pilot study to determine the long-term safety of inhaled AmBisome administration of drug and generate the preliminary data on the effectiveness of this drug to prevent aspergillus colonization.

详细描述

In this pilot study, our main aims are:

  1. To determine the safety of once weekly Inhaled AmBisome prophylaxis in preventing the development of Aspergillus colonization in lung transplant recipients at one year of prophylaxis.
  2. To generate the preliminary data on the efficacy of Inhaled AmBisome (Astellas) loading dose (1mg/kg/day for four days) initially followed by q weekly dosage to complete 1 year in lung transplant recipients as compared to no prophylaxis by assessing the rate of fungal colonization/infections between the groups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
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

  • Single or double lung transplant recipients who are at least one year out of transplantation.
  • Age >18yrs of age
  • Able to understand and complete informed consent.

排除标准

  • Pregnant woman or woman capable of bearing children, who will not perform urine pregnancy test.
  • Nursing mothers.
  • Subjects with hypersensitivity to Amphotericin deoxycholate or liposomal Amphotericin.
  • Subjects with a past history of bronchospasm associated with aerosol drug use.
  • Subjects with active bacterial or viral infection as defined by the current use of non-prophylactic antibiotic anti-viral medications.
  • Subjects treated with cytolytic medications (Campath /Thymoglobulin) within the last month.
  • Subjects with an FEV1< 30% Predicted or FVC% <30%.
  • Subjects requiring supplemental oxygen.
  • Receipt of Inhaled or IV Amphotericin B within last 30 days.
  • Subjects with known fungal infection as per MSG Criteria on therapy with antifungal drugs or diagnosed on the day of bronchoscopy.
  • Current use of azoles active against molds (Voriconazole, itraconazole, posaconazole) for the prophylaxis.
  • Serum creatinine > 150 mmol/L on the day of clinic visit.
  • Liver enzymes ALT/ AST/ Alkphos greater than two times upper limit of normal.
  • Concurrent intravenous aminoglycoside use.
  • Subjects with fever > 38.2°C.
  • Subjects on mechanical ventilation.
  • Expected survival less than 6 months.
  • Re-transplants and heart/lung transplant patients.

研究组 & 干预措施

Control

Active Comparator

Standard of care group. Medication as prescribed by the primary physician would be used by this group. Such medications might include azoles as voriconazole

干预措施: Regular standard of care medication (Drug)

liposomal amphotericin B (AmBisome ®)

Experimental

Inhaled Liposomal preparation of Amphotericin B.

干预措施: Ambisome ® (Drug)

结局指标

主要结局

Pulmonary Function

时间窗: Day 1 to 12 months

Assess pulmonary function measurements i.e. changes in FEV1 (Forced Expiratory Volume 1), changes in FVC (Forced Vital Capacity) while receiving inhaled liposomal amphotericn B.

Symptoms

时间窗: Day 1 to 12months

Assess onset of symptoms including headache, dizziness and fatigue, fever, nausea, vomiting, wheezing, cough, shortness of breath, and taste preservation, while receiving inhaled liposomal amphotericin B

Renal or Hepatic dysfunction and Neutropenia

时间窗: Day 1 to 12 months

Assess the development of renal or hepatic dysfunction and neutropenia by measuring serum creatinine liver enzymes and white blood cells

次要结局

  • Presence of Invasive fungal infection(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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