Postoperative pain relief
Conditions
Interventions
Control group:Provide sufentanil for postoperative analgesia
Experimental group:Provide postoperative analgesia with Tagilidine
Sponsors
Yantai Yuhuangding Hospital
Eligibility
Sex/Gender
Male
Age
30 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. ASA classification I-III, age 30-65 years; 2. 19kg/m^2<BMI<24k g/m^2; 3. Patients undergoing robot-assisted laparoscopic radical prostatectomy; 4. After fully understanding the purpose and significance of this experiment, I voluntarily participate in this trial and have signed the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Allergic to the related medication; 2. Patients with a history of drug or alcohol abuse; 3. Patients with combined hearing and vision impairments or cognitive dysfunction; 4. Individuals with severe heart, lung, liver, or kidney dysfunction; 5. Postoperative ICU patient.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Area under the curve of the visual analog scale (VAS) for pain at rest and during activity within 24 hours postoperatively; | — |
Secondary
| Measure | Time frame |
|---|---|
| Ramsay sedation score at 24 hours post-surgery;Itching;Number of respiratory suppressions;number of rescue analgesic doses within 0-24 hours;Total number of PCA pump presses in 0-24 hours;total amount of rescue analgesics within 0-24 hours;Athens Insomnia Scale on 1 day before surgery, the day of surgery, and 1 day after surgery;time to first rescue analgesia after surgery;Number of vomiting episodes;Nausea and vomiting Apfel score; | — |
Countries
China
Contacts
Public ContactCuicui Yu
Yantai Yuhuangding Hospital
Outcome results
None listed