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Effect of Changes in Endotracheal Tube Cuff Pressure on Postoperative Pharyngolaryngeal Complications in Robotic Surgery

E

Ege University

Status

Completed

Conditions

Prostatic Neoplasms
Robot-Assisted Radical Prostatectomy

Treatments

Other: Continuous Monitoring of Endotracheal Tube Cuff Pressure

Study type

Observational

Funder types

Other

Identifiers

NCT07242144
EUTF 23-7/3

Details and patient eligibility

About

The goal of this observational study is to evaluate how changes in endotracheal tube (ETT) cuff pressure during robot-assisted radical prostatectomy (RARP) affect postoperative throat-related symptoms. The main question the study aims to answer is: Do pneumoperitoneum and the steep Trendelenburg position used in robotic prostate surgery increase ETT cuff pressure and lead to a higher incidence of postoperative pharyngolaryngeal complications such as sore throat, hoarseness, or dysphagia? This study includes 50 male patients undergoing elective radical prostatectomy under general anesthesia, with 25 patients in the open surgery group and 25 in the robotic-assisted group. The ETT cuff pressure is initially adjusted to the lowest level that prevents air leakage (20-35 cmH#O) and is continuously monitored throughout surgery. Measurements are recorded at specific intraoperative time points related to pneumoperitoneum and positioning. After surgery, patients are evaluated at 2 and 24 hours postoperatively for throat-related symptoms such as sore throat, hoarseness, dysphagia, and cough. The results are expected to clarify whether intraoperative factors unique to robotic surgery contribute to increased cuff pressure and postoperative discomfort, emphasizing the importance of continuous cuff pressure monitoring and timely adjustment for patient safety.

Full description

Endotracheal tube (ETT) cuff pressure management is critical in maintaining airway safety during general anesthesia. Excessive cuff pressure may cause mucosal ischemia and postoperative complications such as sore throat, hoarseness, and dysphagia, while insufficient pressure can lead to air leakage and aspiration risk. During robot-assisted laparoscopic radical prostatectomy (RARP), patients are placed in a steep Trendelenburg position with pneumoperitoneum, which may significantly affect airway mechanics and ETT cuff pressure due to increased intrathoracic and airway pressures. This observational study aims to investigate how intraoperative factors unique to robotic surgery-particularly pneumoperitoneum and Trendelenburg positioning-affect ETT cuff pressure and postoperative pharyngolaryngeal outcomes. Fifty adult male patients scheduled for elective radical prostatectomy under general anesthesia are included. Twenty-five undergo open surgery, and twenty-five undergo robotic-assisted surgery. After intubation, the ETT cuff is inflated to the minimal occlusive volume (20-35 cmH#O) and monitored continuously throughout the procedure. Cuff pressure measurements are obtained at defined intraoperative time points, including after pneumoperitoneum, following positioning, and periodically during surgery. Postoperative evaluation includes structured interviews at 2 and 24 hours after extubation to document throat-related symptoms such as sore throat, hoarseness, dysphagia, and cough. The study seeks to provide practical evidence on whether robotic surgical positioning and pneumoperitoneum contribute to elevated cuff pressure and subsequent airway discomfort. These findings may highlight the need for continuous cuff pressure monitoring and adjustment during robot-assisted procedures to improve patient safety and postoperative comfort.

Enrollment

50 patients

Sex

Male

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male patients aged 40 to 80 years

    • Classified as American Society of Anesthesiologists (ASA) physical status I-II
    • Scheduled for elective robot-assisted laparoscopic radical prostatectomy (RALP) or open radical prostatectomy under general anesthesia
    • Able to understand the study procedure and provide written informed consent

Exclusion criteria

  • • Emergency surgery

    • Upper or lower respiratory tract infection within 10 days before surgery
    • ASA physical status > III
    • Obstructed or kinked intraoperative endotracheal tube
    • Risk of aspiration (e.g., gastroesophageal reflux, full stomach)
    • Preoperative sore throat or existing pharyngolaryngeal symptoms
    • Body mass index (BMI) > 35 kg/m²

Trial design

50 participants in 2 patient groups

Robot-Assisted Radical Prostatectomy (RALP)
Description:
Patients undergoing robot-assisted laparoscopic radical prostatectomy under general anesthesia with a steep Trendelenburg position and pneumoperitoneum
Treatment:
Other: Continuous Monitoring of Endotracheal Tube Cuff Pressure
Open Radical Prostatectomy (ORP)
Description:
Patients undergoing open radical prostatectomy under general anesthesia without Trendelenburg position or pneumoperitoneum.
Treatment:
Other: Continuous Monitoring of Endotracheal Tube Cuff Pressure

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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