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临床试验/NCT04116970
NCT04116970
进行中(未招募)
不适用

Prospective Trial to Analyze Endobronchial Ultrasound-Guided Transbronchial Needle-Aspiration (EBUS-TBNA) Samples Obtained With and Without Suction

Ohio State University Comprehensive Cancer Center1 个研究点 分布在 1 个国家目标入组 50 人2020年8月31日

概览

阶段
不适用
干预措施
Bronchoscopy
疾病 / 适应症
Lung Carcinoma
发起方
Ohio State University Comprehensive Cancer Center
入组人数
50
试验地点
1
主要终点
Number of samples collected via endobronchial ultrasound-guided transbronchial needle-aspiration with suction
状态
进行中(未招募)
最后更新
2个月前

概览

简要总结

This trial studies how well endobronchial ultrasound-guided transbronchial needle-aspiration (EBUS-TBNA) with suction works in obtaining samples from patients with suspected lung cancer that has spread to the nodal. EBUS-TBNA samples obtained with additional suction may help to improve material-amounts and decrease blood contamination in the samples.

详细描述

PRIMARY OBJECTIVES: I. To evaluate if suction applied with a vacuum syringe during EBUS-TBNA sampling helps to obtain more material for molecular analyses. OUTLINE: Patients undergo bronchoscopy with EBUS-TBUA first without and then with applied vacuum.

注册库
clinicaltrials.gov
开始日期
2020年8月31日
结束日期
2026年6月15日
最后更新
2个月前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

责任方
Principal Investigator
主要研究者

Peter Kneuertz

Principal Investigator

Ohio State University Comprehensive Cancer Center

入排标准

入选标准

  • Computed tomography (CT)-scan finding suspicious for lung cancer with nodal metastases
  • Clinically stable to undergo diagnostic workup by bronchoscopy with endobronchial ultrasound

排除标准

  • Pregnant female
  • Prisoners
  • Patients with contraindication for EBUS such as non-reversible anticoagulation

研究组 & 干预措施

Diagnostic (bronchoscopy with EBUS-TBNA with/without vacuum)

Patients undergo bronchoscopy with EBUS-TBUA first without and then with applied vacuum.

干预措施: Bronchoscopy

Diagnostic (bronchoscopy with EBUS-TBNA with/without vacuum)

Patients undergo bronchoscopy with EBUS-TBUA first without and then with applied vacuum.

干预措施: Ultrasound-Guided Transbronchial Needle Aspiration

结局指标

主要结局

Number of samples collected via endobronchial ultrasound-guided transbronchial needle-aspiration with suction

时间窗: Up to 3 years

The qualitative data will have a set number of variable to follow and will be converted to quantitative data. Data will be analyzed using Microsoft Excel, SAS, or SPSS. After checking the normality of the data, all non-parametric data will be converted to parametric data. Appropriate tests for categorical and continuous data will be used. Categorical variables will be compared using Chi-square or Fisher?s Exact test. Normally distributed variables will be compared using Student-T-test and one way analysis of variance. Non-parametric test will include Mann Whitney U test and Kruskal Wallis test. A two tailed p value of \< 0.05 will be considered significant.Sample weight (microgram) and visual blood contamination score (0 = no visible blood, 1 = light red shading, 2 = red shading) of endobronchial needle aspiration biopsies obtained with and without suction.

研究点 (1)

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