跳至主要内容
临床试验/NCT06596655
NCT06596655招募中不适用

Implementation of Low-Cost Single-Use Flexible Bronchoscopes for Routine Interventional Pulmonary Procedures: A Feasibility Study

Beth Israel Deaconess Medical Center1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2025年5月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
20
试验地点
1
主要终点
Incidence of crossover from SUFB to RFB (at the discretion of the clinical bronchoscopist)

研究概览

简要总结

The goal of this pilot single-arm crossover trial is to investigate the feasibility and safety of using single-use flexible bronchoscopes (SUFB) for routine diagnostic and therapeutic interventional pulmonary procedures instead of reusable flexible bronchoscopes (RFB). The main questions it aims to answer are:

Was a decision to crossover from SUFB to RFB (at the discretion of the clinical bronchoscopist) made ?

Bronchoscopist's assessment of the SUFB for each procedure (using a Likert scale 0-10) including:

  1. Overall assessment
  2. Scope quality
  3. Scope handling
  4. Scope maneuverability
  5. Tool compatibility
  6. Suction
  7. Lavage
  8. Safety
  9. Image quality

Participants will undergo bronchoscopy with single use bronchoscopes.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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

  • Age 18 or older
  • Able to provide informed consent.

排除标准

  • Emergent procedure
  • Study subjects have any diseases or conditions that interferes with safe completion of the biopsy including: cardiopulmonary instability; sensitivity to drugs that could be administered during bronchoscopy; active anticoagulation or antiplatelet therapy (warfarin, direct Xa inhibitors, thrombin inhibitors, low molecular weight heparin, unfractioned heparin, clopidogrel) not held adequately prior to the procedure; uncontrolled blood dyscrasias; concurrent pneumothorax or bullae.

研究组 & 干预措施

Use of single use bronchoscope

Experimental

干预措施: Single use bronchoscope (Device)

结局指标

主要结局

Incidence of crossover from SUFB to RFB (at the discretion of the clinical bronchoscopist)

时间窗: During the procedure

次要结局

未报告次要终点

研究者

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

Adnan Majid, MD

Chief, Section of Interventional Pulmonology, Division of Thoracic Surgery and Interventional Pulmonology,

Beth Israel Deaconess Medical Center

研究点 (1)

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