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NCT06596655

Single Use Bronchoscopes for Interventional Pulmonology

Recruiting now NA Last updated 13 February 2026
What this trial tests

NA trial testing Single use bronchoscope in Bronchoscopic Interventions in 20 participants. Currently enrolling.

Timeline
23 May 2025
Primary endpoint
1 May 2026
1 October 2027

Quick facts

Lead sponsorBeth Israel Deaconess Medical Center
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment20
Start date23 May 2025
Primary completion1 May 2026
Estimated completion1 October 2027
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Beth Israel Deaconess Medical Center

Who can join

18 and older, any sex, with Bronchoscopic Interventions. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Beth Israel Deaconess Medical Center trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06596655.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing