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临床试验/NCT02973139
NCT02973139已完成不适用

Fibrinolytic Therapy Versus Medical Thoracoscopy for Treatment of Pleural Infection: A Randomized Clinical Trial

Beth Israel Deaconess Medical Center2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2017年7月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
2
主要终点
Duration of hospital stay after intervention

研究概览

简要总结

The purpose of this prospective randomized clinical trial is to compare two currently accepted standard-of-care treatment strategies: Medical thoracoscopy as compared to instillation of intrapleural tissue Plasminogen Activator (TPA) and human recombinant Deoxyribonuclease (DNase) for the management of empyema or complex parapneumonic effusion (CPPE) in adults.

详细描述

Background: Pleural infection (empyema or complex parapneumonic effusion (CPPE)) represents one of the most common clinical diagnoses encountered in clinical practice in the United States (US) It is associated with substantial morbidity and mortality despite advances in medical diagnostic and therapeutic strategies.

Objective: Compare two standard of care treatments: TPA/DNase vs early medical Thoracoscopy

Methods: We will conduct a prospective randomized clinical trial. We plan to enroll a total of 80 patients and randomize them to either Medical Thoracoscopy group or Fibrinolytic Therapy group.

Follow-up will be daily until hospital discharge and at 6 and 12 weeks in the outpatient setting

Primary Outcome: Duration of hospital stay after intervention

研究设计

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

  • Subjects >18 years old with:
  • Evidence of empyema or complex parapneumonic effusion

排除标准

  • Age <18 years
  • Pregnancy
  • Inability to give informed written consent
  • Previous thoracic surgery or thrombolytic therapy for pleural infection
  • Medical thoracoscopy cannot be performed within 48 hours
  • Hemodynamic instability or severe hypoxemia
  • Non corrected coagulopathy
  • Homogeneously echogenic effusion on pleural ultrasonography

结局指标

主要结局

Duration of hospital stay after intervention

时间窗: 12 week follow up period

Number of days hospitalized

次要结局

  • Change in pleural fluid volume on Chest CT scan prior to randomization (day 0) to prior to chest tube removal measured by radiologist blinded to treatment allocation using image J software(12 week follow up period)
  • Number of days with chest drainage(12 week follow up period)
  • Total length of hospital stay(12 week follow up period)
  • Failure rate of assigned treatment necessitating intervention(12 week follow up period)
  • Adverse events(12 week follow up period)
  • In hospital and 30-day mortality(30 days)
  • Inflammatory biomarker (CRP) from randomization (day 0), at 6 weeks and 12 weeks respectively(at randomization and at 6 and12 week follow up visit)
  • Total costs of each treatment modality(6 and 12 week follow up period)

研究者

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

Adnan Majid

MD FCCP

Beth Israel Deaconess Medical Center

研究点 (2)

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