Actively Recruiting
Surveillance Versus Bronchoscopy After Airway Stenting
Led by Icahn School of Medicine at Mount Sinai · Updated on 2025-04-20
50
Participants Needed
1
Research Sites
64 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Randomized, pilot study that evaluates surveillance bronchoscopy versus no surveillance for patients that undergo tracheobronchial stenting
CONDITIONS
Official Title
Surveillance Versus Bronchoscopy After Airway Stenting
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All adult patients that undergo central airway (trachea, main stem bronchi and bronchus intermedius) stenting.
You will not qualify if you...
- Inability to obtain informed consent due to cognitive, neurologic or psychiatric impairment.
- Lobar or segmental stents alone
- Terminally ill patients considered too sick to undergo a follow-up surveillance bronchoscopy
- Stent insertion as a trial for excessive central airway collapse (as the duration of these stents is only 1-2 weeks)
- Patients with a tracheostomy (as these patients can undergo frequent in-line suctioning that can affect the outcomes being assessed)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The Mount Sinai Health System
New York, New York, United States, 10029
Actively Recruiting
Research Team
A
Axel Duval, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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