跳至主要内容
临床试验/NCT07685977
NCT07685977尚未招募不适用

Advanced Robotic Techniques and Rapid Onsite Evaluation for Minimally Invasive Diagnosis and Next-Generation Sequencing: the ARTEMIS Trial.

Vanderbilt University Medical Center8 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2026年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
400
试验地点
8
主要终点
Strict diagnostic yield, defined as the proportion of procedures that result in acquisition of lesional tissue.

研究概览

简要总结

ARTEMIS is a multicenter randomized controlled trial. The goal is to understand whether rapid onsite evaluation during robotic assisted bronchoscopy improves the diagnostic performance of the procedure or not.

详细描述

Pulmonary nodules are an incredibly common finding, with millions incidentally detected in the US every year. Biopsy is often needed for diagnosis. Robotic assisted bronchoscopy (RAB) with integrated cone beam computed tomography (CBCT) has achieved diagnostic yields exceeding 80% in some studies, significantly higher than traditional methods without advanced imaging, due to the added ability to correct alignment of the bronchoscopy catheter with the target lesion in real-time. Given this, the added value of rapid on-site cytologic evaluation (ROSE) with modern bronchoscopy is an area of debate. ROSE involves immediate intraprocedural microscopic assessment of biopsy specimens (typically by a cytotechnologist) to confirm adequacy of biopsy samples for malignant diagnosis during the bronchoscopy. This study will aim to test the hypothesis that modern bronchoscopy done without ROSE guidance is non-inferior to bronchoscopy with ROSE available. Patients undergoing RAB to biopsy a lung lesion will be approached for enrollment and assigned to either ROSE vs no ROSE if they agree to participate. Randomization will be revealed before procedures are started. All decisions regarding procedure tools, techniques, and patient management will be per usual care and at the discretion of the treating physician.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Double (Participant, Outcomes Assessor)

盲法说明

It is not possible to blind the bronchoscopist given the nature of the intervention. However, patients and thoracic pathologists (outcome adjudicators) will remain blinded.

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

  • ≥ 18 years of age at time of bronchoscopy
  • Undergoing robotic assisted bronchoscopy to biopsy a pulmonary lesion

排除标准

  • Declines to participate or inability to provide informed consent.
  • Clinician determination that the use of ROSE is required or contraindicated for the optimal care of an individual patient
  • Patient enrolled in another trial that requires ROSE for PPL biopsy
  • Patient previously consented for this trial
  • Pregnant or incarcerated patients

结局指标

主要结局

Strict diagnostic yield, defined as the proportion of procedures that result in acquisition of lesional tissue.

时间窗: 7 days post procedure

Lesional tissue is defined by the presence of specific pathological findings that readily explain the presence of a pulmonary lesion. The following common pathological findings are pre-specified: 1. Malignancy 2. Specific benign pathologic findings including: organizing pneumonia, frank purulence/robust neutrophilic inflammation with a pathogen isolated, granulomatous inflammation, hamartoma, amyloidoma or other uncommon causes of peripheral pulmonary lesions with distinctive pathological patterns.

次要结局

  • Sufficiency of malignant specimens for Next-Generation Sequencing(30 days post procedure)

研究者

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

Rafael Paez

Assistant Professor of Medicine

Vanderbilt University Medical Center

研究点 (8)

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