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New treatment option for Bronchoscopy
Official title Randomized Controlled Trial of Multi-Patient CT-Derived Digital Twin Anatomical Variability Training to Shorten the Clinical Learning Curve for Bronchoscopy
ClinicalTrials.gov ID: NCT07718451
What this study is testing
- What it's testing
- This study aims to determine whether multi-patient CT-derived digital twin anatomical variability training can shorten the early clinical learning curve of novice bronchoscopists compared with conventional anatomically uniform bronchoscopy simulation training.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 75
You may be able to join if
- Trainee Participants:
- Residents, fellows, or specialty trainees in pulmonary medicine, critical care medicine, thoracic surgery, anesthesiology, or related specialties...
- Previously performed ≤5 flexible bronchoscopies as primary operator.
- No prior formal bronchoscopy simulation training course experience.
- Able and willing to provide written informed consent and permit use of training logs, procedural videos, Ontario Bronchoscopy Assessment Tool (OBAT)...
You likely can't join if
- Trainee Participants:
- Previously performed \>5 flexible bronchoscopies or previously completed a structured bronchoscopy simulation training program.
- Planned departure from the training program during the study period or anticipated inability to complete follow-up through at least clinical cases...
- Unable to participate in simulation training or unwilling to permit procedural video recording.
- Significant additional bronchoscopy training exposure outside the study protocol; such cases may not necessarily be excluded but will be documented...
- Emergency bronchoscopy, intubated intensive care unit patients, severe hypoxemia, or significant hemodynamic instability.
See the full eligibility criteria
- Trainee Participants:
- Residents, fellows, or specialty trainees in pulmonary medicine, critical care medicine, thoracic surgery, anesthesiology, or related specialties whose training programs require flexible bronchoscopy training.
- Previously performed ≤5 flexible bronchoscopies as primary operator.
- No prior formal bronchoscopy simulation training course experience.
- Able and willing to provide written informed consent and permit use of training logs, procedural videos, Ontario Bronchoscopy Assessment Tool (OBAT) scores, and clinical learning curve data for research purposes...
- Age ≥18 years.
- Scheduled to undergo elective low-risk or low-to-moderate-risk diagnostic flexible bronchoscopy.
- Clinically suitable for supervised novice-performed airway inspection, bronchoalveolar lavage, simple brushing, or other low-risk sampling procedures considered safe by the supervising bronchoscopist.
- Able to understand and provide written informed consent and willing to complete pre-procedure anxiety and post-procedure experience questionnaires.
- Trainee Participants:
- Previously performed \>5 flexible bronchoscopies or previously completed a structured bronchoscopy simulation training program.
- Planned departure from the training program during the study period or anticipated inability to complete follow-up through at least clinical cases 1-30.
- Unable to participate in simulation training or unwilling to permit procedural video recording.
- Significant additional bronchoscopy training exposure outside the study protocol; such cases may not necessarily be excluded but will be documented and addressed in sensitivity analyses. Patient Participants:
- Emergency bronchoscopy, intubated intensive care unit patients, severe hypoxemia, or significant hemodynamic instability.
- Therapeutic bronchoscopy, complex central airway stenosis, high bleeding risk, procedures requiring advanced treatment techniques, or cases considered unsuitable for novice participation.
- Complex sampling procedures such as EBUS-TBNA, transbronchial lung biopsy, or cryobiopsy will not be included in the primary endpoint case set and may be analyzed separately as exploratory subgroups or in future studies.
- Refusal of trainee participation or refusal of procedural recording and/or questionnaire completion.
The study team makes the final eligibility decision.
Where it's taking place
- Beijing, Beijing Municipality, China
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 75 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Beijing, Beijing Municipality, China. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.