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Clinical Trials/NCT01350674
NCT01350674
Suspended
Not Applicable

Role of EBUS-TBNA (Endobronchial Ultrasound Transbronchial Needle Aspiration- in Diagnosing Tuberculosis in Mediastinal and/or Hilar Lymph Nodes

Centre Hospitalier Universitaire Saint Pierre1 site in 1 country50 target enrollmentDecember 2010
ConditionsTuberculosis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tuberculosis
Sponsor
Centre Hospitalier Universitaire Saint Pierre
Enrollment
50
Locations
1
Primary Endpoint
The ratio of tuberculosis in mediastinal lymph nodes
Status
Suspended
Last Updated
7 years ago

Overview

Brief Summary

This is an observational prospective study. Role of EBUS-TBNA (endobronchial ultrasound transbronchial needle aspiration) is evaluated to diagnose tuberculosis in mediastinal and/or hilar lymph nodes.

The investigators analyse the specificity and sensibility of this technique to diagnose tuberculosis in mediastinal and/or hilar lymph nodes.

Patients with mediastinal and/or hilar lymph nodes on X-ray or CT thorax where a tuberculosis is the most probable cause and who have no parenchymal lesions suspected for tuberculosis and without other lymph nodes that are more easily accessible or palpable will be included in this study.

Registry
clinicaltrials.gov
Start Date
December 2010
End Date
March 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Centre Hospitalier Universitaire Saint Pierre
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patients with enlarged mediastinal and/or hilar lymph nodes on chest CT highly suspicious of tuberculosis (suggestive clinical history, suggestive echographic findings ...) without pulmonary lesions suspicious for tuberculosis or in whom the first evaluation with sputum examination, classical bronchoscopy, induced sputum didn't result in any diagnosis.
  • patients aged 18 years or older
  • patients need to sign the consent form after reading the information form

Exclusion Criteria

  • synchronic pulmonary lesions suspicious for tuberculosis or already proven tuberculosis by microscopic exam, PCR-technique and/or culture
  • other affected ganglionary sites more easily accessible (cervical, supraclavicular, axillary ... region)

Outcomes

Primary Outcomes

The ratio of tuberculosis in mediastinal lymph nodes

Time Frame: 8 weeks

Study Sites (1)

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