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临床试验/NCT00548730
NCT00548730
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A Clinical Comparison Trial of White Light Bronchoscopy, Autofluorescence Bronchoscopy and Narrow Band Imaged Bronchoscopy

Antonios Likourezos1 个研究点 分布在 1 个国家2007年10月1日
适应症Lung Cancer

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Lung Cancer
发起方
Antonios Likourezos
试验地点
1
主要终点
Degree of correlation between three different bronchoscopic images
状态
撤回
最后更新
2年前

概览

简要总结

The purpose of the study is to compare the three methods of bronchoscopic imaging to determine what combination is optimum to identify neoplastic mucosal abnormalities. The ability to decrease the rate of false-positive and false negative findings of bronchoscopy also will be studied for each spectroscopic technique separately and for their combination.

详细描述

Patients with known or suspected malignancies of the lung and with a medical indication for a bronchoscopy will be invited to participate in the study. All patients must be over 18 years old and must sign informed consent. The endoscopic examination of the bronchial tree will be performed using a commercially available flexible fluorescence bronchoscope (11004BI; Karl Storz; Culver City, CA) and the flexible white light video-bronchoscope (BF-T180; Olympus; Center Valley, PA). Images obtained will be photographed using both video recordings and parallel images of white light and imaged bronchoscopy. These digital images will be electronically stored and evaluated at a later time. Biopsies will be obtained of all suspected abnormalities. These will be correlated with the images. Images will be identified as normal, suspect or abnormal based upon each modality independently, paired with the spectral image and all three combined. The control will be an area considered normal by all modes of bronchoscopy. Images will be graded at the time of bronchoscopy. Later, all images will be graded in a blind fashion by two independent bronchoscopists. Standard statistical analysis using paired Student's t test will be applied. We anticipate that the combination of one or more imaged bronchoscopy techniques will increase accuracy by 25%. Power calculation to detect such a difference will require 140 abnormal specimens. If 50% of patients examined have an abnormality, the study population will need to be around 300 patients. Histopathology reports will be obtained on all specimens. Abnormal results will be discussed with the individual patient and appropriate procedures will be performed based upon best medical practices. These procedures and patient follow-up are beyond the scope of the study.

注册库
clinicaltrials.gov
开始日期
2007年10月1日
结束日期
2009年5月31日
最后更新
2年前
研究类型
Observational
性别
All

研究者

发起方
Antonios Likourezos
责任方
Sponsor Investigator
主要研究者

Antonios Likourezos

Research Administration Director

Maimonides Medical Center

入排标准

入选标准

  • Patients with lung abnormalities that have an indication for bronchoscopy

排除标准

  • Inability to tolerate bronchoscopy

结局指标

主要结局

Degree of correlation between three different bronchoscopic images

时间窗: One day

次要结局

  • Elimination of false positives and negative bronchoscopic examinations for neoplasia(One day)

研究点 (1)

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