跳至主要内容
临床试验/JPRN-jRCT1052210051
JPRN-jRCT1052210051尚未招募未知

A study on the utility of conventional diameter forceps in endobronchial ultrasound-guided intranodal forceps biopsy

akai Toshiyuki0 个研究点目标入组 60 人开始时间: 2021年7月16日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
> 20age old 至 ot applicable(—)
性别
All

入选标准

  • 1) Patients with suspected primary lung cancer of clinical stage IIIA or higher, including enlarged hilar and mediastinal lymph nodes, satisfying all of the imaging studies in 1. and clinical findings in 2.
  • 1. enlargement of 10 mm or more in short diameter on chest contrast CT or accumulation of SUVmax 2.50 or more on FDG-PET. 2.
  • 2) Clinically suspected primary lung cancer, or already diagnosed as primary lung cancer by other tests.
  • 2) Patients who are scheduled for EBUS-TBNA and EBUS-IFB for 1).
  • 3) Patients who are 20 years old or older.
  • 4) Patients who have given written consent to participate in the study.
  • Translated with www.DeepL.com/Translator (free version)

排除标准

  • 1) For the purpose of staging.
  • 2) Patients with suspected sarcoidosis or lymphoproliferative disease, either clinically or by other tests.
  • 3) Patients with poorly controlled complications (unstable angina, post-acute myocardial infarction, severe bronchial asthma, active pulmonary infection, heart failure, bleeding tendency, etc.), psychosis or psychiatric symptoms that interfere with daily life, or dementia.
  • 4) Other cases that the registered physician deems inappropriate for inclusion.
  • Translated with www.DeepL.com/Translator (free version)

研究者

发起方
akai Toshiyuki

相似试验