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临床试验/NCT05399082
NCT05399082已完成不适用

A Study to Evaluate the Feasibility of Robotic Bronchoscopy-guided Miniature Cryoprobe Biopsy of Peripheral Pulmonary Lesions

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年8月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
30
试验地点
2
主要终点
Ability to Successfully Obtain Sample

研究概览

简要总结

This research is being done to evaluate the feasibility, and biopsy quality, of using a 1.1mm disposable cryoprobe that is passed through the working channel of the Ion Robotic bronchoscope to collect biopsy tissue.

研究设计

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

  • Patient clinically meets indication for peripheral lung nodule biopsy and has been scheduled for robotic bronchoscopy.
  • Lesion Criteria:
  • Pulmonary nodules of 8-50mm in largest dimension.

排除标准

  • Patients with known bleeding diathesis; Platelet count < 50,
  • Current use of systemic anticoagulation or antiplatelet therapy without the ability to hold therapy for the recommended amount of time prior to an invasive procedure (aspirin monotherapy is acceptable).
  • Inability or unwillingness to give informed consent.
  • Pregnant or nursing females, or females of child-bearing potential who decline a pregnancy test prior to enrollment.
  • Pulmonary hypertension, defined as a right ventricular systolic pressure > 50 mmHg.
  • Individuals with current or recent systematic conditions, such as, acute kidney injury, or conditions that would mandate anticoagulation, such as a recent coronary stent.
  • International Normalized Ratio (INR) < 1.
  • Do Not Resuscitate (DNR) status; Do Not Intubate (DNI) status.

结局指标

主要结局

Ability to Successfully Obtain Sample

时间窗: Baseline

Number of tissue samples that are considered by the bronchoscopist as adequate for further pathological analysis

次要结局

  • Duration of Biopsy Procedure(Biopsy procedure, approximately 3 hours)
  • Freezing Time for Cryoprobe Biopsies(Biopsy procedure, approximately 60 seconds)
  • Number of Successful Biopsy Attempts(Biopsy procedure, approximately 3 hours)
  • Histological Accessibility Grade(Pathology review, approximately 1 day)
  • Histological Diagnostic Yield(Pathology review, approximately 1 day)
  • Total Histological Area(Pathology review, approximately 1 day)
  • Crush Artifacts(Pathology review, approximately 1 day)
  • Other Pathologic Artifacts(Pathology review, approximately 1 day)
  • Different Tissue Types in the Tissue Specimen(Pathology review, approximately 1 day)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ryan M. Kern

Principal Investigator

Mayo Clinic

研究点 (2)

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