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临床试验/NCT03799809
NCT03799809Unknown2 期

Efficacy of Intrabronchial Voriconazole Instillation for Inoperable Pulmonary Aspergilloma- a Randomized Controlled Trial

All India Institute of Medical Sciences, New Delhi1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年12月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
60
试验地点
1
主要终点
To compare the percentage of patients achieving reduction in hemoptysis in intrabronchial voriconazole with standard medical therapy group vs standard medical therapy alone for inoperable pulmonary aspergilloma at 3 months.

研究概览

简要总结

Pulmonary aspergillomas are a common cause of recurrent hemoptysis which may be moderate to severe in 2 to 50 % of cases and may be life threatening. Surgical resection, though curative, may not be feasible in significant number of patients and also associated significant post op complications. Bronchial artery embolisation (BAE) is effective for acute control of hemoptysis, however recurrences may occur in upto a quarter of subjects over a 1 year period.

Aspergilloma is caused by a fungus hence systemic antifungals seem appropriate choice. However the fungus only partially touch the walls of the cavities containing them and rarely come into contact with the bloodstream. This is the major reason why the systemic administration of antifungal agents is ineffective in eradicating the condition.

If surgical resection is not a treatment option to control recurrent hemoptysis, instillation of antifungal agents in an aspergilloma cavity could be considered(QoE II).The instillation of antifungal directly into the cavity (intra-cavitatory) containing aspergilloma brings the drug in contact with the fungus. Thus may lead to antifungal action and shrinkage or complete disappearance of aspergilloma. This can be achieved either by percutaneous route or bronchoscopically. Percutaneous approaches have been investigated however they can sometimes cause fungal spread in thoracic space resulting in fungal empyema which should be carefully avoided. Endobronchial instillation of antifungals have been investigated and found to be safe and effective in controlling hemoptysis, however published data comprise of case reports or small case series.

Recently we have published our experience of intrabronchial voriconazole in aspergilloma among 82 patients and found to be safe and effective in hemoptysis control, with transient post procedure cough as an adverse effect with no major serious adverse events. Multiple small studies and case reports have published the safety and efficacy of voriconazole. However, a quality data in the form of randomized controlled trial (RCT) is not there. Therefore, we planned this RCT to assess the efficacy of intrabronchial voriconazole in inoperable aspergilloma.

详细描述

Primary Objective : To compare the percentage of patients achieving reduction in hemoptysis in intrabronchial voriconazole with standard medical therapy group vs standard medical therapy alone for inoperable symptomatic pulmonary aspergilloma.

Secondary Objectives:

  1. To compare the percentage of patients who have complete cessation of hemoptysis after 3 months.
  2. To compare the percentage of patients having recurrence of hemoptysis during 3 months follow up.
  3. To compare the severity of hemoptysis during recurrence in both groups.
  4. To compare the change in size of aspergilloma after 3 - 6 months following last intrabronchial voriconazole instillation.
  5. To compare the percentage of patients who need BAE during anytime till 3 - 6months.
  6. To compare the percentage of patients with symptomatic improvement in Dyspnea On Exertion, Cough and recurrent respiratory infections.

Number of Patients: 30 patients in each arm (Intrabronchial voriconazole with Standard medical therapy vs Standard medical therapy alone)

Study Design : Prospective Randomized control study

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
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

  • Patients with mild to moderate hemoptysis AND inoperable aspergilloma/ those unwilling for surgery.
  • Who have no contra-indication of flexible fibre-optic bronchoscopy
  • Age > 18 yrs AND
  • Given the written informed consent to participate in the study.

排除标准

  • Patient who are not fit for FOB (e.g. hemodynamic instability)
  • Patient who have life threatening hemoptysis requiring immediate bronchial artery embolization
  • Patients who have underwent BAE in last 3 months
  • Pregnant woman

研究组 & 干预措施

Voriconazole

Active Comparator

Will receive 400 mg of Intrabronchial Voriconazole every week for 4 weeks along with standard medical therapy.

干预措施: Intrabronchial Voriconazole instillation (Drug)

结局指标

主要结局

To compare the percentage of patients achieving reduction in hemoptysis in intrabronchial voriconazole with standard medical therapy group vs standard medical therapy alone for inoperable pulmonary aspergilloma at 3 months.

时间窗: 3 months follow up

Percentage of patients achieving reduction in hemoptysis in intrabronchial voriconazole with standard medical therapy group vs standard medical therapy alone for inoperable pulmonary aspergilloma at 3 months.

次要结局

  • To compare the percentage of patients having recurrence of hemoptysis during 3 months follow up.(3 months follow up)
  • To compare the severity of hemoptysis during recurrence in both groups.(3 months follow up)
  • To compare the percentage of patients who have complete cessation of hemoptysis after 3 months.(3 months follow up)
  • To compare the change in size of aspergilloma after 3 months following last intrabronchial voriconazole instillation.(3 months follow up)
  • To compare the percentage of patients who need BAE during anytime till 3 months.(3 months follow up)
  • To compare the percentage of patients with symptomatic improvement in Dyspnea On Exertion, Cough and hemoptysis.(3 months follow up)

研究者

发起方
All India Institute of Medical Sciences, New Delhi
申办方类型
Other
责任方
Principal Investigator
主要研究者

DR SACHIN D

senior resident

All India Institute of Medical Sciences, New Delhi

研究点 (1)

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