Study Comparing Endotracheal Tube Suctioning to No Suctioning During Recovery From General Anesthesia in Adults Undergoing Elective Surgery
Led by Mahidol University · Updated on 2026-01-12
408
Participants Needed
1
Research Sites
12 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating whether skipping tracheal suctioning right before removing a breathing tube is as safe as routine suctioning for adult patients aged 18 to 90 who undergo planned surgery under general anesthesia with endotracheal intubation. The study aims to see if avoiding suctioning affects early oxygen levels after the tube is removed and whether it impacts cough severity, sore throat, and other related side effects.
Participants are randomly divided into two groups one receiving routine suctioning inside the trachea and throat just before extubation, and the other receiving suctioning only in the throat without inserting the suction catheter into the trachea. All patients receive standard anesthesia care and are monitored in the post-anesthesia care unit PACU for 60 minutes after extubation. Airway symptoms and satisfaction are checked again 24 hours after surgery.
During the study, participants will have their oxygen levels monitored closely for the first hour after extubation, along with assessments of coughing, sore throat severity, nausea, vomiting, and any extubation-related problems. Researchers will also record oxygen therapy needs and patient satisfaction at 24 hours. Safety monitoring continues up to 6 hours post-PACU arrival. Overall participation involves the surgery day and a follow-up at 24 hours post-surgery.
CONDITIONS
Brief Title
Endotracheal Tube Suctioning Versus No Suctioning During Emergence From General Anesthesia
Research Team
S
Saowaluk Sotananan, Doctor of Medicine
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Adults aged 18 to 90 years with ASA physical status I-III
Scheduled for elective surgery under general anesthesia requiring endotracheal intubation
Planned tracheal extubation in the operating room at the end of surgery
You will not qualify if you...
Inability to provide informed consent or significant language barrier
Known obstructive sleep apnea, active pneumonia, or chronic pulmonary disease
Body mass index over 35 kg/m²
Pregnancy or increased aspiration risk
Scheduled for maxillofacial, head and neck, or airway surgery
Anticipated surgery longer than 3.5 hours
Anticipated difficult airway with two or more predictors or history of difficult intubation
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Treatment
Duration - During surgery and emergence from anesthesia
Participants receive either routine endotracheal suctioning or oropharyngeal suctioning only immediately prior to extubation during general anesthesia.
1 procedure visit (in-person)
Post-operative Follow-up
Duration - Up to 24 hours after surgery
Participants are monitored for postoperative desaturation, coughing, sore throat, oxygen therapy needs, nausea and vomiting, and extubation-related adverse events for up to 6 hours after arrival in the post-anesthesia care unit (PACU). Patient satisfaction is assessed approximately 24 hours after surgery.
1 follow-up visit in the first hour and 1 visit at 24 hours post-surgery
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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Published Research Related To This Trial
Major complications of airway management in the UK: results of the Fourth National Audit Project of the Royal College of Anaesthetists and the Difficult Airway Society. Part 1: anaesthesia.
Pharmacological methods for reducing coughing on emergence from elective surgery after general anesthesia with endotracheal intubation: protocol for a systematic review of common medications and network meta-analysis.