Comparing two methods for double-lumen tube intubation in thoracic surgery
Video Versus Direct Laryngoscopy for Double-lumen Tube Tracheal Intubation in Thoracic Surgery
This study is testing whether using a video camera for intubation works better than the traditional method for patients having thoracic surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 916 (estimated) |
| Ages | 18 Years to 90 Years |
| Sex | All |
| Sponsor | Hospital Clinico Universitario de Santiago Academic / other |
| Locations | 4 sites (A Coruña and 3 other locations) |
| Trial ID | NCT06401486 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of videolaryngoscopy versus the traditional Macintosh laryngoscope for performing double-lumen tube tracheal intubation in patients undergoing thoracic surgery. It is a prospective multicenter randomized trial that will assess the success rate of intubation on the first attempt using these two techniques. The larger size and stiffness of the double-lumen tube can complicate intubation, making this comparison critical for improving patient outcomes in thoracic procedures.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 years or older who are scheduled for thoracic surgery and require intubation with a double-lumen tube.
Not a fit: Patients who are pregnant, lactating, or require alternative intubation methods will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the success rate of intubation on the first attempt, reducing complications and improving patient safety during thoracic surgeries.
How similar studies have performed: Previous studies have indicated that videolaryngoscopy may improve intubation success rates, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18 years or older. * Patients admitted to any of the participating hospitals in the study who are undergoing thoracic surgery. * Need for intubation with a double-lumen tube. Exclusion Criteria: * Pregnant or lactating women. * Individuals who do not have the capacity to understand their participation in the study. * Need for tracheal intubation with a device other than videolaryngoscopy or direct laryngoscopy (fiberoptic bronchoscope, tracheostomy...).
Where this trial is running
A Coruña and 3 other locations
- Complexo Hospitalario Universitario de A Coruña — A Coruña, Spain (Recruiting)
- Complexo Hospitalario Universitario de Santiago de Compostela — Santiago de Compostela, Spain (Recruiting)
- Hospital Universitario La Fe de Valencia — Valencia, Spain (Recruiting)
- Complexo Hospitalario Universitario Vigo — Vigo, Spain (Recruiting)
Study contacts
- Principal investigator: Manuel Taboada, Ph.D. — Clinical University Hospital of Santiago de Compostela
- Study coordinator: Manuel Taboada, Ph.D.
- Email: manutabo@yahoo.es
- Phone: +34-678195618
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.