Postoperative chronic pain
Conditions
Interventions
trial group:Pump remifentanil during surgery
control group:Do not use remifentanil during surgery
Sponsors
Tianjin Medical University General Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1: Men and women over the age of 18 2: ASA classification is grade I, II, or III 3: patients who will undergo thoracoscopic surgery under general anesthesia 4: patients understand this study clearly,voluntarily participate in, and sign an informed consent form by themselves
Exclusion criteria
Exclusion criteria: 1: Patients have a history of chronic pain or acute pain before surgery 2: Patients have been taking painkillers for a long time 3: Patients have severe liver and kidney dysfunction 4: Patients are in a state of depression and anxiety 5: Patients are pregnant or lactating women 6: Patients are allergic to the drugs involved in the study 7: Patients have participated in other drug clinical trials as a subject within the past 3 months 8: Researcher consider that patients should not participate in this trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of postoperative chronic pain; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative acute pain score;The quality of sleep;Anxiety and Depression score; | — |
Countries
China
Contacts
Public ContactXie,Yegong
Tianjin Medical University General Hospital
Outcome results
None listed