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Recruiting NCT06767696

NCT06767696 Effect of Neck Hyperextension on Endotracheal Tube Cuff Pressure in Children

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Clinical Trial Summary
NCT ID NCT06767696
Status Recruiting
Phase
Sponsor Ankara Ataturk Sanatorium Training and Research Hospital
Condition Endotracheal Cuff
Study Type OBSERVATIONAL
Enrollment 120 participants
Start Date 2025-01-06
Primary Completion 2025-06-06

Eligibility & Interventions

Sex All sexes
Min Age 2 Years
Max Age 18 Years
Study Type OBSERVATIONAL
Interventions
Cuff pressure measurement

Eligibility Fast-Check

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What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 120 participants in total. It began in 2025-01-06 with a primary completion date of 2025-06-06.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Introduction: Patients undergoing surgery under general anaesthesia are frequently intubated with an endotracheal tube (ETT). The safety margin of ETT cuff pressure is between 20-30 cmH2O. Inadequately inflated cuff (\<20 cmH2O) may cause secretions in the mouth, foreign bodies, bleeding due to surgery to escape into the trachea and/or air leakage. As a result of air leakage, the effect of mechanical ventilation decreases, end-tidal CO2 measurement cannot be performed accurately, and inhalation anaesthetics leak into the operating room. An overinflated cuff (\>30 cmH2O) may affect tracheal mucosa blood flow. This may result in tracheal stenosis, tracheoesophageal fistula or tracheal rupture. There may be significant changes in cuff pressure during endotracheal intubation because cuff pressure can be affected by changes in head and neck position. Due to all these situations, controlling ETT cuff pressure is very important for patient health and safety. For ETT cuff pressure control; manual palpation of the pilot balloon, listening for the disappearance of an audible air leak, inflating the cuff with minimal occlusive pressure to a peak inflation pressure of 20-22 cmH2O during positive pressure ventilation, inflating the cuff until the airway is closed by maintaining a continuous positive airway pressure of 20 cmH2O, or cuff manometers are commonly used applications. Although cuff manometers can be used to guide the monitoring of cuff pressure, their use and availability is not mandatory in many institutions around the world (due to the large number of anaesthetic areas, it is not possible to have a manometer everywhere). Therefore, in anaesthetic practice, cuff pressure is monitored manually or using a manometer at regular intervals during the operation. Aim/Hypothesis: H0: Endotracheal tube cuff pressure does not change with hyperextension position given to the neck during adenoidectomy, tonsillectomy or adenotonsillectomy surgery. H1: Endotracheal tube cuff pressure changes with hyperextension position given to the neck during adenoidectomy, tonsillectomy or adenotonsillectomy surgery. Material-Methods: The study will include patients between the ages of 2-18 years who will undergo adenoidectomy, tonsillectomy or adenotonsillectomy after obtaining informed consent from their parents. Routine practice will be followed for induction and maintenance of anaesthesia. Patients monitored in the operating room according to the standard American Society of Anesthesiologists (ASA) protocol will be orotracheally intubated with an ETT of appropriate internal diameter after induction of anaesthesia by the anaesthesiologist responsible for the patient. After the tube placement of the intubated patients is confirmed by the responsible anaesthesiologist, the ETT cuff will be measured and recorded by the responsible investigator with a cuff manometer (VBM Medizintechnik, GmbH, Germany) while the head and neck are in the neutral position (T0). When the patients are given the head-neck hyperextension position in which the surgery will be performed by the surgical team responsible for the patient's surgery, the pressure measurements will be repeated by the responsible investigator (T1). At the end of the operation, when the head and neck are returned to the neutral position, the tubular cuff pressure will be measured by the responsible investigator for the last time (T2). Patients between 2-18 years of age who underwent adenoidectomy, tonsillectomy or adenotonsillectomy surgery will be included in the study. Patients with head and neck mobility restriction, patients who have had neck surgery before, and patients with body mass index (BMI) \> 35 kg/m2 will be excluded from the study.

Eligibility Criteria

Inclusion Criteria: * Patients aged 2-18 years * undergoing adenoidectomy, tonsillectomy or adenotonsillectomy surgery Exclusion Criteria: * Patients with restricted head and neck mobility, * patients with intraoperative complications, * patients with previous neck surgery, * patients with BMI \> 35 kg/m2

Contact & Investigator

Central Contact

ERBİL TÜRKSAL, Specialist

✉ drerbilturksal@hotmail.com

📞 530 228 1319

Principal Investigator

Erbil Türksal, Specialist

PRINCIPAL INVESTIGATOR

University of Health Sciences, Ankara Atatürk Sanatorium Training and Research Hospital

Frequently Asked Questions

Who can join the NCT06767696 clinical trial?

This trial is open to participants of all sexes, aged 2 Years or older, up to 18 Years, studying Endotracheal Cuff. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06767696 currently recruiting?

Yes, NCT06767696 is actively recruiting participants. Contact the research team at drerbilturksal@hotmail.com for enrollment information.

Where is the NCT06767696 trial being conducted?

This trial is being conducted at Ankara, Turkey (Türkiye).

Who is sponsoring the NCT06767696 clinical trial?

NCT06767696 is sponsored by Ankara Ataturk Sanatorium Training and Research Hospital. The principal investigator is Erbil Türksal, Specialist at University of Health Sciences, Ankara Atatürk Sanatorium Training and Research Hospital. The trial plans to enroll 120 participants.

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