Actively Recruiting

Age: 19Years - 90Years
All Genders
NCT06887335

Deep Sedation With Pre-emptive Endotracheal Intubation for Advanced Bronchoscopy Procedures

Led by Pusan National University Yangsan Hospital · Updated on 2025-05-31

203

Participants Needed

1

Research Sites

90 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Bronchoscopy is crucial for diagnosing and treating respiratory diseases and is recommended under sedation. Deep sedation improves patient comfort and procedural efficiency, especially in complex cases, by reducing movement and coughing. However, it carries risks of respiratory depression and airway obstruction, potentially requiring premature termination or urgent intubation. Determining the optimal timing for intubation can be challenging despite proper monitoring. To enhance safety, the investigator has performed bronchoscopy under deep sedation with preemptive intubation for years, sharing this experience with other hospitals. This study aims to evaluate its safety and feasibility through a multicenter prospective observational approach.

CONDITIONS

Official Title

Deep Sedation With Pre-emptive Endotracheal Intubation for Advanced Bronchoscopy Procedures

Who Can Participate

Age: 19Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients requiring a bronchoscopy-assisted procedure for diagnostic or therapeutic purposes
  • Individuals who voluntarily consent to participate in the clinical study and sign a written informed consent form
Not Eligible

You will not qualify if you...

  • Patients who have experienced acute myocardial infarction or acute stroke within the past six weeks
  • Patients with contraindications to bronchoscopy such as severe respiratory or cardiovascular comorbidities
  • Patients with a history of allergy to benzodiazepines, propofol, fentanyl, or flumazenil
  • Patients with genetic disorders including galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption
  • Patients with a severe hypersensitivity reaction to dextran 40
  • Patients with a history of acute angle-closure glaucoma
  • Pregnant women
  • Prisoners
  • Patients with psychiatric disorders
  • Patients classified as ASA Physical Status IV or V by the American Society of Anesthesiologists
  • Any other patients deemed unsuitable for the clinical study by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Pusan National University Yangsan Hospital

Yangsan, South Korea

Actively Recruiting

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Research Team

H

Hee Yun Seol, MD, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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