Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06596655

Single Use Bronchoscopes for Interventional Pulmonology

Led by Beth Israel Deaconess Medical Center · Updated on 2026-02-13

20

Participants Needed

1

Research Sites

123 weeks

Total Duration

On this page

Sponsors

B

Beth Israel Deaconess Medical Center

Lead Sponsor

O

Olympus

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this pilot single-arm crossover trial is to investigate the feasibility and safety of using single-use flexible bronchoscopes (SUFB) for routine diagnostic and therapeutic interventional pulmonary procedures instead of reusable flexible bronchoscopes (RFB). The main questions it aims to answer are: Was a decision to crossover from SUFB to RFB (at the discretion of the clinical bronchoscopist) made ? Bronchoscopist's assessment of the SUFB for each procedure (using a Likert scale 0-10) including: 1. Overall assessment 2. Scope quality 3. Scope handling 4. Scope maneuverability 5. Tool compatibility 6. Suction 7. Lavage 8. Safety 9. Image quality Participants will undergo bronchoscopy with single use bronchoscopes.

CONDITIONS

Official Title

Single Use Bronchoscopes for Interventional Pulmonology

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 or older
  • Able to provide informed consent.
Not Eligible

You will not qualify if you...

  • Emergency procedure
  • Pregnancy
  • Any condition that would make biopsy unsafe, including cardiopulmonary instability
  • Sensitivity to drugs used during bronchoscopy
  • Active use of blood thinners not properly stopped before the procedure
  • Uncontrolled blood disorders
  • Current pneumothorax or lung bullae

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

Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States, 02215

Actively Recruiting

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Research Team

C

Christine Conley

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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