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临床试验/NCT02765087
NCT02765087Unknown不适用

Diagnostic Utility of the E-Nose for Pleural TB

Universidad Central de Venezuela2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2015年1月最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
100
试验地点
2
主要终点
Sensitivity and Specificity of the device for the diagnosis of Tuberculosis Pleural effusion

研究概览

简要总结

The purpose of this study is to determine the diagnostic utility of the device 'Electronic Nose' for Pleural TB, which is a Extra pulmonary TB form, compared with pleural biopsy, the current gold standard.

详细描述

The aim of the study is to determine the diagnostic utility of the device 'Electronic Nose' for Pleural TB, which is a Extra pulmonary TB form.

The patient who qualified for the study, according to the inclusion criteria, after consenting, will be guided through and oriented survey for risk factors, then a complete physical exam, and after that, the patient will breathe for 5 minutes trough the device, which stores the patient information, that later will be download to a computer and will be send to the server's manufacturer company, in Netherlands.

During and after the use of the device, investigators determine the adverse effects of the intervention, according to the CTCEA.

Investigators use the pleural biopsy, which is the gold standard, to determine the diagnostic utility of the test. And, will compare the results with other tests currently perform as the regular diagnostic routine, such as Chest CT, adenosine deaminase value of pleural fluid and cytomorphologic & cytochemistry of the pleural fluid.

Patient Registries will be keep in an electronic database, as well as handwriting history, with the backup copy in the records of the hospital in which the patient was admitted.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
15 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Severe compromise of the general condition
  • Not capable to exhaled through the E-nose.
  • No possibility to follow-up.
  • By discretion of the research team.

研究组 & 干预措施

Pleural TB

Experimental

This group consist of patients with TB pleural effusion.

Intervention:

  1. Inform Consent
  2. Medical History
  3. E-Nose Device
  4. Chest CT
  5. Cytomorphologic & Cytochemistry of pleural Fluid.
  6. Adenosine Deaminase value of pleural Fluid.

干预措施: Medical History (Other)

Pleural TB

Experimental

This group consist of patients with TB pleural effusion.

Intervention:

  1. Inform Consent
  2. Medical History
  3. E-Nose Device
  4. Chest CT
  5. Cytomorphologic & Cytochemistry of pleural Fluid.
  6. Adenosine Deaminase value of pleural Fluid.

干预措施: E-Nose (Device)

Pleural TB

Experimental

This group consist of patients with TB pleural effusion.

Intervention:

  1. Inform Consent
  2. Medical History
  3. E-Nose Device
  4. Chest CT
  5. Cytomorphologic & Cytochemistry of pleural Fluid.
  6. Adenosine Deaminase value of pleural Fluid.

干预措施: Chest CT (Other)

Pleural TB

Experimental

This group consist of patients with TB pleural effusion.

Intervention:

  1. Inform Consent
  2. Medical History
  3. E-Nose Device
  4. Chest CT
  5. Cytomorphologic & Cytochemistry of pleural Fluid.
  6. Adenosine Deaminase value of pleural Fluid.

干预措施: Pleural Fluid Analysis (Other)

Control

Active Comparator

Patients with pleural effusion with different aetiologies than Tuberculosis.

Intervention:

  1. Inform Consent
  2. Medical History
  3. E-Nose Device
  4. Chest CT
  5. Cytomorphologic & Cytochemistry of pleural Fluid.
  6. Adenosine Deaminase value of pleural Fluid.

干预措施: Medical History (Other)

Control

Active Comparator

Patients with pleural effusion with different aetiologies than Tuberculosis.

Intervention:

  1. Inform Consent
  2. Medical History
  3. E-Nose Device
  4. Chest CT
  5. Cytomorphologic & Cytochemistry of pleural Fluid.
  6. Adenosine Deaminase value of pleural Fluid.

干预措施: E-Nose (Device)

Control

Active Comparator

Patients with pleural effusion with different aetiologies than Tuberculosis.

Intervention:

  1. Inform Consent
  2. Medical History
  3. E-Nose Device
  4. Chest CT
  5. Cytomorphologic & Cytochemistry of pleural Fluid.
  6. Adenosine Deaminase value of pleural Fluid.

干预措施: Chest CT (Other)

Control

Active Comparator

Patients with pleural effusion with different aetiologies than Tuberculosis.

Intervention:

  1. Inform Consent
  2. Medical History
  3. E-Nose Device
  4. Chest CT
  5. Cytomorphologic & Cytochemistry of pleural Fluid.
  6. Adenosine Deaminase value of pleural Fluid.

干预措施: Pleural Fluid Analysis (Other)

结局指标

主要结局

Sensitivity and Specificity of the device for the diagnosis of Tuberculosis Pleural effusion

时间窗: 1 year

次要结局

  • Adverse Effects related to the use of the device, according to the CTCEA(1 year)

研究者

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

Jacobus H. de Waard

Chief of Tuberculosis Laboratory

Universidad Central de Venezuela

研究点 (2)

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