Oral and maxillofacial tumors, postoperative sore throat
Conditions
Interventions
Test group:Local spray administration of the throat
Control group:Conventional aerosol inhalation administration
Sponsors
Peking University Hospital of Stomatology
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Patients with oral and maxillofacial tumors with indwelling gastric tube after full surgery; 2. Age>=18 years old, able to understand and cooperate with the research requirements; 3. Patients without pharyngeal discomfort and upper respiratory tract infection 2 weeks before surgery; 4. Have not received treatment and surgery for the external throat site of this study 1 month before surgery; 5. Conscious; 6. No language and communication barriers; 7. No history of budesonide drug allergy; 8. Voluntarily participate in this study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Patients with difficulty in tracheal intubation and unsuccessful intubation at one time; 2. Patients who are allergic to therapeutic drugs; 3. Patients with diabetes mellitus who are unstable after monitoring and control of blood glucose (fasting >=8mmol/L, postprandial >=11mmol/L); 4. Patients diagnosed with chronic pharyngitis or tracheitis in the past three months; 5. Other treatment methods are used in the research process, which affects the efficacy of the patient; 6. Patients who withdrew from the study on their own in the middle of the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative sore throat; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative comfort level; | — |
Countries
China
Contacts
Public ContactHongmei Guo
Peking University Hospital of Stomatology
Outcome results
None listed