Postoperative pain
Conditions
Interventions
Experimental group:Dezocine combined with lidocaine
Control group:Sufentantil
Sponsors
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1?A signed and dated informed consent form; 2?Committing to comply with the research procedures and cooperate with the implementation of the entire research process; 3?In accordance with the diagnosis of perianal diseases, with the intention to undergo elective perianal surgery. 4?Patients aged 18 to 65 years;
Exclusion criteria
Exclusion criteria: 1?Pregnant or breastfeeding; 2?Preoperative liver and kidney function abnormalities; 3?Patients with coronary heart disease; 4?ASA classification of grade 4 or higher; 5?Physically dependent on anesthetic drugs; 6?Allergic to opioids;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of Recovery-40; | — |
Secondary
| Measure | Time frame |
|---|---|
| VAS Digital Pain Score; | — |
Countries
China
Contacts
Public ContactHaiyan Zhang
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Outcome results
None listed