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A randomized prospective cohort study of the use of video endotracheal tube with endobronchial blocker versus endotracheal tube with endobronchial blocker

A randomized prospective cohort study of the use of video single lumen endotracheal tube with endobronchial blocker versus single lumen endotracheal tube with endobronchial blocker

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068983
Enrollment
Unknown
Registered
2023-03-03
Start date
2023-03-03
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

None listed

Interventions

video endotracheal tube group:video endotracheal tube with endobronchial blocker
endotracheal tube group:endotracheal tube with endobronchial blocker

Sponsors

Shanghai Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective thoracic surgery requiring intraoperative single-lung ventilation OLV (including various surgical types such as open surgery/thoracoscopic surgery, various surgical sites such as lung/esophagus/mediastinum, and various anesthesia methods such as general anesthesia/general anesthesia combined with epidural/general anesthesia combined with nerve block); 2. Aged 18-80 years; 3. American Society of Anesthesiologists (ASA) Grade I-III; 4. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Serious systemic diseases: such as BMI>35, systemic infection such as sepsis, respiratory diseases such as severe COPD and asthma, circulatory diseases such as malignant arrhythmias and decompensated heart failure affecting hemodynamic stability, and severe abnormal liver and kidney function; 2. Other thoracic surgeries were performed within 4 weeks; 3. Suspected history of tuberculosis; 4. Contraindication of occlude placement: abnormal tracheobronchial anatomy, such as distortion of the left main bronchus caused by descending thoracic aorta or tumor compression; Surgeries involving the left main bronchus, such as left lung transplantation, left tracheobronchial rupture repair, left lung resection, left sleeve resection, etc.; 5. Suspected/known difficult airway: including a history of head and neck malignancy or radiotherapy, known difficulty intubating, Mallampati Grade 4, mouth opening < 3.5 cm, or jaw spacing < 6.5 cm; 6. Surgery requiring other lung isolation devices or techniques (tracheotomy, nasal intubation); 7. High risk of reflux aspiration; 8. Pregnant or lactating patients; 9. Other conditions deemed unsuitable for inclusion by the researchers.

Design outcomes

Primary

MeasureTime frame
incidence of hypoxia;

Secondary

MeasureTime frame
intubation time;intraoperative frequency of fibrobronchoscope;time (T1) for recomfirming tube position and time (T2) for adjustment time after positioning;blood gas was measured, PO2 and PCO2 were recorded, and oxygenation index was calculated during 30min of one-lung ventilation;total numer of bronchoscope;subjective score of lung collapse quality (5min and 15min evaluation);total cost;

Countries

China

Contacts

Public ContactWu Jingxiang

Shanghai Chest Hospital

Wjx1132@163.com+86 136 4162 9197

Outcome results

None listed

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