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Clinical Trial ● Currently Recruiting NCT07168408

Procedural Skills Transfer in Bronchoscopy

Procedural Skills Transfer in Bronchoscopy — Recruiting • Respiratory / COPD / Asthma • NCT07168408.

📅 21 Sep 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
NCT ID
NCT07168408
Sponsor
University of Edinburgh
Start
2025-05-06
ClinicaliQ Trial Snapshot
  • Procedural Skills Transfer in Bronchoscopy — Recruiting • Respiratory / COPD / Asthma • NCT07168408.
  • What is being tested: This feasibility study captures bronchoscopy procedural data (CT scans and endoscopy videos) from patients and bronchoscopists over three years to evaluate skills transfer and procedural standardisation in bronchoscopy practice.
  • Patient eligibility overview: The study recruits 300 patients undergoing clinically-indicated bronchoscopy procedures, alongside bronchoscopists of varying experience levels, to ensure diverse procedural and technical expertise is captured.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

Brief summary The goal of this Feasibility study is to capture bronchoscopy data from patients (Group1) and bronchoscopists (Group 2) over a period of three years. The investigators wish to collect the pre-procedure CT scans and endoscopy videos of 300 patients. Up to 20 bronchoscopists will take part in the study Primary outcomes 1. To collect imaging data from patients undergoing routine bronchoscopy procedures 2. To collect movement data from clinicians performing the routine bronchoscopy procedures using a sensory Glove Secondary outcomes 1. Integrate the data gathered with procedure guidelines…

Eligibility Snapshot
  • Group 1 * over 16 years of age * patients identified as requiring a bronchoscopy by their clinician * patients must have had a CT scan in the 8 weeks prior to the procedure * capacity to consent

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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