About this trial
This clinical trial aims to understand whether a visual double-lumen intubation tube can improve the first-attempt success rate and reduce complications compared to a standard double-lumen tube. The trial primarily aims to answer the following questions:
Does a double-lumen tube improve the first-attempt success rate?
Does a visual double-lumen tube reduce the likelihood of obstruction of the right upper lobe bronchial opening?
Does a visual double-lumen tube require fewer adjustments during surgery?
Do patients with visual double-lumen tubes experience fewer perioperative complications compared to those with standard double-lumen tubes?
Participants will:
Use a visual double-lumen tube partially and a standard double-lumen tube partially.
Record the perioperative status of all patients.
Eligibility criteria
Qualifiers
Age: at least 18 years old, gender is not limited.
American Anesthesiologists Association (ASA) Grade I-III;
Elective Video-Assisted Thoracoscopic Lobectomy.
Informed consent of the patient or family member.
Disqualifiers
Patients with contraindications for right double-lumen tube insertion (such as right bronchial tumor).
The patient has known tracheobronchial anatomical abnormalities
Patients previously diagnosed or suspected of having airway difficulty.
Patients who need rapid sequence induction.
Trial design
Treatments tested in this trial
- visible double-lumen tube
- lumen intubation tube
Treatment groups
Sponsors and collaborators
Diansan Su
Lead sponsor
Zhejiang University
Sponsor institution
Ningbo No.2 Hospital
Collaborator
Affiliated Hospital of Jiaxing University
Collaborator