Postoperative fatigue in patients undergoing abdominal surgery
Conditions
Interventions
Trial Group:Starting from the first day after surgery, oral administration of Ginseng Guben Oral Liquid or nasogastric feeding via gastric tube, 10ml each time, once in the morning and once in the eve
Control Group:Starting from the first day after surgery, placebo liquid was orally administered or nasogastric feeding was administered via a gastric tube, 10ml each time, once in the morning and once
Sponsors
The Second Hospital, Cheeloo College of Medicine, Shandong University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Patients aged >= 18 years and <= 70 years, without surgical contraindications, and in the perioperative period; 2. Hepatobiliary surgery patients who undergo open surgery and fourth level laparoscopic surgery; 3. Patients without serious internal medicine diseases, mental illnesses, or a history of major surgeries; 4. Patients who are conscious, have no communication difficulties, have good compliance, and voluntarily accept the survey.
Exclusion criteria
Exclusion criteria: 1. Patients with severe heart, lung, brain, liver, and kidney dysfunction after surgery; 2. Patients who experience significant postoperative complications and are unable to take medication regularly; 3. Patients with poor postoperative compliance who are expected to have difficulty in normal follow-up; 4. Patients who cannot tolerate drugs or experience significant side effects and give up participating in clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Perioperative fatigue level; | — |
Secondary
| Measure | Time frame |
|---|---|
| Fatigue state;Fatigue expression rating; | — |
Countries
China
Contacts
Public ContactLiu Chongzhong
The Second Hospital, Cheeloo College of Medicine, Shandong University
Outcome results
None listed