Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Hyperangulated vs standard videolaryngoscopy vs direct laryngoscopy for double-lumen tube intubation

Official title: Evaluation of Efficacy and Safety of Hyperangulated and Standard Curvature Blade Video Laryngoscopy Versus Direct Laryngoscopy for Double-Lumen Endobronchial Tube Intubation

Run by Trakya University · NCT07614529 · Data updated 2026-11-12

This trial tests three laryngoscopy methods to place a double-lumen tube in adults having thoracic surgery with one-lung ventilation.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment180 (estimated)
SponsorTrakya University
Academic / other
Locations1 site (Edirne, Edirne)
StatusRecruiting
StartedJune 15, 2026
Main results expectedNovember 15, 2028
Study endsJanuary 15, 2029
Registry record updatedOctober 30, 2026
Trial IDNCT07614529 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older undergoing elective thoracic surgery needing one-lung ventilation and double-lumen intubation, with ASA I–III and able to consent.

Probably not a fit

Patients with ASA IV or higher, emergency cases, or anticipated difficult airway or contraindications to any of the three techniques may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective, randomized, open-label study compares three laryngoscopy approaches for double-lumen endobronchial tube placement in adults undergoing elective thoracic surgery requiring one-lung ventilation. It includes three arms: C-MAC hyperangulated (D-blade) videolaryngoscopy, C-MAC Macintosh blade videolaryngoscopy, and direct Macintosh laryngoscopy. The primary outcome is time from end of mask ventilation to fiberoptic confirmation of correct tube position; secondary outcomes include glottic view quality, intubation difficulty, number of attempts, and need for auxiliary maneuvers. The trial is conducted at Trakya University Hospital and aims to inform best practices for safer, more efficient DLT placement in thoracic anesthesia.

Why it matters

Potential benefit: If successful, the study could identify the fastest and easiest method for DLT placement, potentially reducing airway trauma and anesthesia-related complications.

How similar studies have gone: Previous work suggests varying success with videolaryngoscopy versus direct laryngoscopy for complex intubations; this study provides direct comparison in the DLT context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18 years or older
* Written informed consent obtained prior to surgery
* ASA physical status class I, II, or III
* Scheduled for elective thoracic surgery requiring one-lung ventilation and double-lumen endobronchial intubation

Exclusion Criteria:

* Age under 18 years
* Refusal or inability to provide informed consent
* ASA physical status class IV or above
* Emergency surgery
* Anticipated difficult airway, defined by any of the following: Mallampati score 4, thyromental distance less than 6.5 cm, restricted mouth opening, or BMI greater than 30 kg/m²
* History of upper airway surgery
* Significant upper airway obstruction or stridor
* Pregnancy

Where it's running

  • Trakya University Hospital
    Edirne, Edirne, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • BMI-Adjusted PEEP During One-Lung Ventilation in Thoracic Surgery

    This trial tests whether adjusting PEEP based on BMI during one-lung ventilation in thoracic surgery improves outcomes compared with a fixed PEEP.

    Recruiting Fundación de Investigación Biomédica - Hospital Universitario de La Princesa · Barcelona, Catalonia and 3 other locations · NCT07851740

  • AirGo Respiratory Monitoring During Lung Resection

    Patients undergoing lung resection will wear the AirGo device to continuously monitor breathing before and after surgery to see if it helps track ventilation alongside standard checks.

    Recruiting Fondazione IRCCS Policlinico San Matteo di Pavia · Pavia, Lombardy · NCT07838025

  • Frailty-focused prehabilitation before heart surgery

    This study tests a home-based, frailty-tailored prehabilitation program for adults 65+ waiting 5 weeks or more for heart surgery to see if it improves fitness, frailty, heart-related function, nutrition, inflammation, quality of life, and hospital outcomes.

    Recruiting The University of Hong Kong · Hong Kong · NCT07824700

  • Wireless home prehabilitation for older adults with NSCLC awaiting lung surgery

    This study tests whether a personalized home exercise program guided by wearable devices can improve lung function for older NSCLC patients preparing for curative lung surgery.

    Recruiting West China Hospital · Chengdu, Sichuan · NCT07809763

  • Transdermal buprenorphine patch added to multimodal pain relief after VATS

    This study tests whether adding a 5 mcg/hour buprenorphine patch to standard pain relief after unilateral VATS reduces pain in adults.

    Recruiting Clínica Dávila · Santiago, Santiago Metropolitan · NCT07733128

  • Continuous ESP Block vs Thoracic Epidural for Preventing Chronic Pain After Thoracotomy

    This study compares whether a continuous erector spinae plane block can better prevent chronic post-thoracotomy pain than the current standard thoracic epidural analgesia in adults undergoing elective thoracic surgery.

    Recruiting Meir Medical Center · Kfar Saba · NCT07677540

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.