Actively Recruiting

Age: 18Years +
All Genders
ID05681962

Practice of Oxygenation and Respiratory Support During Fiberoptic Bronchoscopy The Oxy-FOB Observational Study

Led by University Magna Graecia · Updated on 2024-12-30

10000

Participants Needed

1

Research Sites

154 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how oxygen and breathing support are currently used in adult patients undergoing Fiberoptic Bronchoscopy (FOB). This is an observational study that aims to understand different oxygenation and ventilation methods used during FOB across various patient conditions, procedure types, and hospital settings. The study includes adults with respiratory issues such as acute respiratory failure, pneumonia, lung cancer, lung fibrosis, and interstitial lung disease. Participants will undergo the bronchial endoscopy procedure required for their condition. These procedures include toilet bronchoscopy to remove secretions or blood, broncho-aspirate, bronchoalveolar lavage, cytology brushing, biopsy, and endobronchial ultrasound. Researchers will record the type and size of the bronchoscope used and details about sedation and oxygen support methods, such as no support, standard oxygen therapy, high flow nasal cannula, non-invasive ventilation, or mechanical ventilation. During the study, investigators will monitor vital signs throughout the procedure and 15 minutes afterward. They will track any adverse events like oxygen drops, blood pressure changes, heart rhythm problems, or neurological issues. Clinical outcomes such as the need for increased respiratory support or hospital admission will also be recorded. The main outcome measured is the type of oxygenation strategy used during the approximately 30-minute bronchoscopy procedure.

CONDITIONS

Official Title

Practice of Oxygenation and Respiratory Support During Fiberoptic Bronchoscopy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Need for any procedure with flexible FOB
  • Patients can be outpatients in dedicated ambulatories or admitted to any hospital ward or Intensive Care Unit (ICU)
Not Eligible

You will not qualify if you...

  • None

AI-Screening

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Trial Site Locations

Total: 1 location

1

AOU Mater Domini

Catanzaro, Italy

Actively Recruiting

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Research Team

F

Federico Longhini, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

5

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Published Research Related To This Trial