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Application of visual single lumen tracheal catheter combined with bronchial occluder in minimally invasive coronary artery bypass grafting surgery

Application of visual single lumen tracheal catheter combined with bronchial occluder in minimally invasive coronary artery bypass grafting surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072124
Enrollment
Unknown
Registered
2023-06-03
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

coronary heart disease

Interventions

Visual single lumen tracheal catheter combined occluder(VBB):Using a visual single lumen tracheal catheter combined with occluder for tracheal intubation
video double-lumen tube(VDLT): Using a visible dual lumen tracheal catheter for tracheal intubation

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Patients who require continuous coronary artery bypass grafting surgery with small incisions (including single or multiple branches); ? Age 18-80 years old; ? The American Society of Anesthesiologists (ASA) grading is III to IV; ? Sign an informed consent form;

Exclusion criteria

Exclusion criteria: ? Contraindications to the placement of occluder: such as anatomical abnormalities of trachea and bronchus, tracheobronchial tumors, and operations involving the main bronchus (pneumonectomy); ? Patients with morbid obesity [body mass index (BMI)>35 kg/m2]; ? Severe systemic diseases such as sepsis and other systemic infections, severe COPD (pre operative lung function examination showing forced expiratory volume in the first second (FEV1)<50% of the expected value), respiratory diseases such as asthma, and severe liver and kidney dysfunction; ? Suspected or known difficult airway: including a history of head and neck malignant tumors or radiation therapy, known history of difficult intubation, modified Mallampati grade III-IV, mouth opening<3.5 cm or nail chin spacing<6.5 cm, etc; ? Unable to cooperate with the researcher for any reason;

Design outcomes

Primary

MeasureTime frame
Tracheal intubation time;

Secondary

MeasureTime frame
Number of intubations and first success rate;Intraoperative lung collapse score;Total number of corrections and total correction time;Airway plateau pressure and peak pressure during 10 and 30 minutes of single lung ventilation;Incidence of hypoxemia;Postoperative complications;QoR-15 scores at 24 and 48 hours after extubation;Collection of blood samples and detection of biochemical indicators;Hemodynamic indicators;

Countries

China

Contacts

Public ContactYongzheng Han

Peking University Third Hospital

hanyongzheng@163.com+86 152 0130 4460

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026