Tracheal Tube and Swallowing After Head and Neck Surgery
NCT05738421
Summary
The present study was designed as a cross-sectional observational study providing the enrollment of tracheostomized patients undergoing major oncological surgery for head-neck cancer. Aims: * to provide objective data on the bolus transit during swallowing in tracheostomized patients with tracheal tube and without tracheal tube closing directly the tracheal stoma with a plaster, in order to sustain the choice to preserve the TT in dysphagic patients after oncologic surgery for more security during swallowing rehabilitation or adjuvant treatment. * to evaluate the features of swallowing, specifically bolus transit, in patients affected by head and neck cancer who underwent major oncological surgery.
Eligibility
Inclusion criteria * Age \>18 years * Tracheal tube diameter of 5.0 mm and outside diameter of 9.4 mm * Tolerance of the tracheal tube capping for almost 48 hours without pathologic desaturation during continue monitoring of SpO2 * Ability to swallow in accordance to the inpatient training program * Ability to suck with a straw without oral leakage Exclusion criteria * Previous head and neck radiotherapy * Patients with nasal tube feeding * Patients with poor cognition or poor general condition or affected by neurological o other nontumor-related dysphagia * Patients total laryngectomized * Patients unable to maintain the orthostatic position
Conditions2
Browse More Trials
Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.
NCT05738421