Patients undergoing elective surgery requiring at least 6 hours of fasting
Conditions
Interventions
Fasting:None
Preoperative Oral Carbohydrate:None
Sponsors
Shandong Institute of Pharmaceutical Research Ethics Committee
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1. Age requirement: The subjects were 18 to 70 years old; 2. Disease status: Elective patients were instructed to maintain a fasting state for a minimum of 6 hours prior to the surgical procedure; 3. Voluntary Participation: Patients were invited to participate in the study on a voluntary basis. After being thoroughly informed about the study objectives, procedures, and potential risks, they were required to sign an informed consent form. Participants must also be willing to adhere to all study requirements, including regular follow-up visits and data collection, which can be completed during the inpatient phase; 4. Nutritional Status: There is no evidence of any impairment in nutrient absorption or metabolism; 5. (ASA) classification: ASA ?-?;
Exclusion criteria
Exclusion criteria: 1. Gastrointestinal Function: Patients with compromised gastrointestinal function, including conditions such as gastroparesis, gastric obstruction, gastroesophageal reflux disease (GERD), peptic ulcer disease, gastric carcinoma, pyloric stenosis, functional dyspepsia, intestinal obstruction, and intestinal ischemia, etc; 2. In conjunction with other comorbidities: individuals diagnosed with diabetes mellitus, as well as those suffering from severe cardiac, pulmonary, hepatic, or renal dysfunction, hypertension, or cerebrovascular accidents; 3. History of allergy: Patients with a documented history of severe allergic reactions to any components of the study interventions, as well as those with a previous history of allergic reactions to narcotic medications. 4. Patients presenting with a mental illness or serious psychological problem (as confirmed by medical history); 5. Investigator judgment: Other factors that the investigator believes may affect the study results or the safety of the participants;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative recovery: fasting blood glucose, fasting triglyceride and TyG;Postoperative recovery: Adverse reactions occurred within 12 hours after surgery;Subjective comfort:Hunger, Thirst, Anxiety; | — |
Secondary
| Measure | Time frame |
|---|---|
| Actual preoperative fasting management;Hospital stay and cost; | — |
Countries
China
Contacts
Public ContactBing Wang
Shandong Institute of Pharmaceutical Research Ethics Committee
Outcome results
None listed