None listed
Conditions
Interventions
Procedure/Surgery : The postoperative oral hydration intervention will be implemented for patients who have sufficiently recovered from general anesthesia. Participants will be divided into two groups
Sponsors
Asan Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Adults aged 18 years or older who are alert, capable of communication, and able to respond to the questionnaire. 2) Patients who demonstrate a willingness to participate in early postoperative oral hydration. 3) Patients classified as ASA-PS (American Society of Anesthesiologists Physical Status) I to III prior to surgery. 4)Patients who voluntarily signed a written informed consent form after receiving a full explanation of the study's purpose, methods, and expected benefits, and who agreed to comply with the treatment and procedures. 5) In the case of vulnerable participants aged 80 years or older, those for whom both the participant and their legal guardian (representative) have directly signed the written informed consent form.
Exclusion criteria
Exclusion criteria: 1) Patients who are unable to cooperate or participate in the study due to delirium or mental confusion. 2) Patients with a potential need for emergency re-operation due to complications such as active bleeding or persistent air leakage. 3) Patients assessed to have a high risk of aspiration due to unstable respiratory status, or those experiencing dysphagia resulting from postoperative laryngeal nerve injury or severe pharyngeal edema. 4) Patients with severe, uncontrolled nausea or recurrent vomiting, posing a risk of symptom exacerbation or aspiration upon oral intake. 5) Patients admitted to the Intensive Care Unit (ICU) following surgery. 6) Elderly patients with underlying conditions that may cause swallowing disorders, such as a history of dementia, Parkinson’s disease, or stroke. Withdrawal Criteria Participants will be withdrawn from the study if they withdraw their consent or refuse to continue participation at any point during the research process.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| thirst | — |
Secondary
| Measure | Time frame |
|---|---|
| oropharyngeal discomfort;nausea and vomiting;Patient Satisfaction | — |
Countries
Korea, Republic of
Contacts
Public ContactJuri Jung
Asan Medical Center
Outcome results
None listed