Actively Recruiting
Site of Tracheal Extubation and Operating Room Efficiency During Robot-assisted Surgery
Led by Peking University First Hospital · Updated on 2026-01-15
218
Participants Needed
1
Research Sites
11 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to evaluate the impact of different extubation strategy on the occupancy time of operating room (OR) and the incidence of adverse events and quality of recovery after robotic-assisted surgery. The investigators hypothesize that extubation in the post-anesthesia care unit (PACU) may reduce OR occupancy time without increasing adverse events or worsening quality of recovery early after robotic-assisted surgery. This strategy may enhance perioperative efficiency while maintaining clinical safety.
CONDITIONS
Official Title
Site of Tracheal Extubation and Operating Room Efficiency During Robot-assisted Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 years or older
- Scheduled for elective robot-assisted laparoscopic surgery under general anesthesia
- Expected tracheal extubation during daytime working hours (before 4:00 PM)
You will not qualify if you...
- Refuse to participate in the study
- Morbid obesity with body mass index 35 kg/m² or higher
- Preoperative diagnosis of obstructive sleep apnea or STOP-Bang score 3 or more with serum bicarbonate 28 mmol/L or higher
- High risk of difficult airway identified before surgery
- Preexisting severe heart rhythm disorders without pacemaker or severe cardiovascular diseases with NYHA class III or higher
- Significant lung function impairment with FEV1/FVC ratio below 70% and total lung capacity or vital capacity below 80% of predicted
- Severe liver dysfunction (Child-Pugh class C), severe kidney dysfunction (eGFR below 30 mL/min/1.73 m²), or ASA physical status class IV or higher
- Preoperative diagnosis of schizophrenia, epilepsy, Parkinson's disease, or myasthenia gravis
- Unable to communicate due to coma, severe dementia, or language difficulties
- Planned postoperative admission to intensive care unit
- Any other conditions deemed unsuitable for study participation
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Peking University Fist Hospital
Beijing, Beijing Municipality, China, 100034
Actively Recruiting
Research Team
D
Dong-Xin Wang, MD, PhD
CONTACT
T
Ting Ding, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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