Image

A Single-center, Prospective Study for Mechanism and Risk Factors of Tracheal Tube-related Tongue Injury

A Single-center, Prospective Study for Mechanism and Risk Factors of Tracheal Tube-related Tongue Injury

Non Recruiting
18-85 years
All
Phase N/A

Powered by AI

Overview

Article Summary

  1. Tracheal tube-related tongue injury is a common clinical complication that would lead to serious events such as dysphagia, respiratory dysfuncion and macroglossia.
  2. There is a lack of qualitative and quantitative risk assessment of tracheal tube-related tongue injury.
  3. This is a protocol of a single-center, prospective, paralled-group clinical trial based on the measurement of dynamic changes in pressure between the tracheal tube and the tongue in different position during the surgery.
  4. The primary endpoint is tracheal tube-related tongue injury, secondary outcomes include the time to first successful recovery of oral intake of fluids and solid food and airway-related events.
  5. This trial aims to find the best indicators for tracheal tracheal tube-related tongue injury and to provide solid basis for optimizing airway protection strategies and surgical positioning.

Description

Background Tracheal tube-related tongue injury can lead to post-intubation pharyngeal dysfunction, postoperative macroglossia, or stridor after extubation. Possible mechanisms include increased oral pressure, obstruction of venous and lymphatic return in the neck, leading to severe throat pain, dysphagia, and respiratory function impairment. There is a lack of indicators and clinical awareness of this issue. Therefore we have designed this study to accurately monitor the tracheal tube-tongue pressure in different surgical position during general anesthesia.

Method This is a prospective, single-center observational study. Fifty-four patients undergoing elective surgery in general anesthesia for more than 2 hours with endotracheal tube applied will be enrolled. Patients will be divided into supine position (Supine group) and the high-risk positions (Flexion group) groups. Dynamic changes in pressure between the tracheal tube and the tongue are measured. All patients will be followed up until 7 days after operation. Primary endpoint is tracheal tube-related tongue injury. Secondary outcomes include the time to first successful recovery of oral intake of fluids and solid food, and airway-related events.

Discussion The study aims to explore the risk factors and pressure thresholds for tracheal tracheal tube-related tongue injury.

Eligibility

Inclusion Criteria:

  1. ASA I-III
  2. Age 18-85 years old
  3. Scheduled for elective surgery with tracheal intubation under general anesthesia, with operation duration ≥2 hours
  4. The intended surgical position will be supine, prone, cervical traction or beach chair position
  5. Obtained informed consent

Exclusion Criteria:

  1. Informed consent is not obtained
  2. Maxillofacial surgeries or other surgeries involving the oral cavity and upper airway
  3. History of head and neck radiotherapy
  4. Deformity, trauma, infection and active bleeding exist in the mouth and tongue
  5. Airway hyperresponsiveness, active asthma, acute exacerbation of chronic obstructive pulmonary disease, laryngeal osteomalacia
  6. Respiratory insufficiency, moderate to severe ventilation or diffusion dysfunction
  7. Existing chronic sore throat, recurrent laryngeal nerve injury, dysarthria, dysphagia, severe gastroesophageal reflux, upper esophageal sphincter dysfunction, cardiac stenosis and other basic diseases
  8. Postoperative total parenteral nutrition therapy is planned

Study details
    Tracheal Tube-related Tongue Injury

NCT05987293

China-Japan Friendship Hospital

20 August 2025

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.