Tonsil adenoid hypertrophy
Conditions
Interventions
Control group:Normal surgical procedure
Sponsors
The Fifth Affiliated Hospital of Sun Yat-sen University
Eligibility
Sex/Gender
All
Age
3 Years to 14 Years
Inclusion criteria
Inclusion criteria: 1. Obtain the consent of the subject's legal guardian, voluntarily participate in this research and abide by the research regulations, agree to the operation, understand and abide by the follow-up plan, and correctly record the scale score, frequency of medication, concomitant medication and adverse event records, etc. The legal guardian voluntarily signs a written informed consent form. If the minor can make a decision of informed consent to participate in the research, he must also voluntarily participate in the research and abide by the research regulations; 2. The age of the subject is 3-14 years old; 3. Gender is not limited, limited to Chinese; 4. Accompanied by varying degrees of snoring and mouth breathing; 5. Meet the indications for tonsil with adenoid hypertrophy surgery; 6. No serious heart, lung, brain disease and metabolic disease; 7. No malnutrition; 8. Normal lung function; 9. No history of tonsil inflammation and upper respiratory tract infection within 3 to 4 weeks; 10. Laboratory test indicators are normal.
Exclusion criteria
Exclusion criteria: 1. Combined with respiratory abnormalities; 2. Morbid or simply obese children; 3. Local anesthetic drug allergy, analgesic drug dependence, local infection injury at the injection site, clinically serious metabolic, cardiovascular, immune, nervous, blood, digestive, cerebrovascular or respiratory system diseases, or any interference with the research in the opinion of the researcher Assessment of outcomes or illnesses affecting subject safety; 4. Currently participating in other clinical research or participating in other clinical research within 30 days, or staff directly involved in this research; 5. Have a history of mental illness, confrontational personality, bad motivation, suspicious or other emotional or intellectual problems, which may affect the informed validity of participating in the research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score;Restlessness score;Hospital stay;Hospitalization expenses; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative complications;Postoperative analgesics;Stress indicators; | — |
Countries
China
Contacts
Public ContactHong Haiyu
The Fifth Affiliated Hospital of Sun Yat-sen University
Outcome results
None listed