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Effect of continuous measurement and adjustment of endotracheal tube cuff pressure on postoperative sore throat in patients undergoing gynecological laparoscopic surgery: a randomised controlled study

Effect of continuous measurement and adjustment of endotracheal tube cuff pressure on postoperative sore throat in patients undergoing gynecological laparoscopic surgery: a randomised controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064792
Enrollment
Unknown
Registered
2022-10-18
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Postoperative sore throat

Interventions

Cuff pressure measurement and adjustment group:Continuous measurement and adjustment of endotracheal tube cuff pressure
Control group:Only continuous measurement without adjustment of endotracheal tube cuff pressure

Sponsors

Beijing Chaoyang Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-65 years; 2. The body mass index (BMI) ranges from 18.0 to 30.0 kg/m ^ 2; 3. The American Society of Anesthesiologists (ASA) is classified as Level I-II; 4. Subjects undergoing elective gynecological laparoscopic surgery who require general anesthesia, tracheal intubation, and mechanical ventilation; 5. Participants must give informed consent to this study before the experiment and voluntarily sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Preoperative cough, sore throat, upper respiratory tract infection; 2. Insert a gastric tube before surgery; 3. Smoking history; 4. History of nausea and vomiting; 5. History of oropharyngeal surgery; 6. The researcher believes that there are any other circumstances that are not suitable for participation in the experiment due to the interests of the subject.

Design outcomes

Primary

MeasureTime frame
The incidence of sore throat at rest within 24 hours after extubation;

Secondary

MeasureTime frame
The incidence of cough within 24 hours after extubation;The incidence of hoarseness within 24 hours after extubation;The incidence of nausea and vomiting within 24 hours after extubation;The intensity of sore throat within 24 hours after extubation;Pain intensity within 24 hours after extubation;

Countries

China

Contacts

Public ContactChen Wang

Beijing Chaoyang Hospital, Capital Medical University, Beijing, China

correspondingauthor@foxmail.com+86 10 85231330

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026