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Non-invasive Ventilation Assisted Fiber-optic Bronchoscopy

Lung Clinical Trial

Official title:
Efficacy and Safety of Using Non-invasive Ventilation Assisted Fiber-optic Bronchoscopy

Clinical Trial Summary

The purpose of this study is the evaluation of using bi-level positive airway pressure ventilation in candidates for fiber-optic bronchoscopy regarding benefits and drawbacks.

Clinical Trial Description

In this study patients who will be candidate for fiber-optic bronchoscopy for diagnostic or therapeutic reasons will be evaluated by the Chest Medicine Department, Mansoura University Hospitals. All patients will be subjected to full history taking, full examination, routine laboratory investigations, arterial blood gases (ABG), chest X-ray, chest computed tomography (CT). Non-invasive ventilation: Group 1 (hypoexemic patient who will undergo bronchoscopy under non- invasive ventilation{NIV}) will be on NIV half an hour prior and throughout the bronchoscopic sampling and after the procedure until reach the baseline criteria, Group 2 (hypoxemic patients who will undergo conventional bronchoscopy ) will be on conventional oxygen therapy half an hour prior and throughout the bronchoscopic sampling and after the procedure until reach the baseline criteria, Group 3 (non- hypoxemic patients who will undergo conventional bronchoscopy ) will be on NIV throughout the bronchoscopic sampling and after the procedure until reach the baseline criteria, Group 4 (non- hypoxemic patients who will undergo conventional bronchoscopy) will be on conventional oxygen therapy throughout the bronchoscopic sampling and after the procedure until reach the baseline criteria. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06115395
Study type Interventional
Source Mansoura University
Contact Walaa Abd El Aziz, MD
Phone 01064904172
Email Wm22446699@gmail.com
Status Recruiting
Phase N/A
Start date July 25, 2020
Completion date October 30, 2025
View Details
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