Acute pain
Conditions
Interventions
control group:Propofol
Sponsors
Yantai Affiliated Hospital of Binzhou Medical College
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. ASA I or II patients; 2. Patients aged 18-60 years old; 3. Patients with body weight of 45-85kg and BMI of 18.5-24kg/m2; 4. Patients undergoing hysteroscopy or hysteroscopic surgery; 5. Patients with clear consciousness and active cooperation can understand the postoperative recovery quality assessment scale, qor-40 emotional scale and so on after a short training.
Exclusion criteria
Exclusion criteria: 1. Patients who are allergic to propofol or to rimazole; 2. Patients with severe cardiac dysfunction; 3. Patients with respiratory tract management difficulties (modified Mahalanobis score is grade IV); 4. Patients with chronic respiratory insufficiency; 5. Patients with severe abnormal liver and kidney function (alanine aminotransferase 3 times higher than normal or creatinine higher than normal); 6. Patients with central nervous system or psychological diseases, history of chronic pain, long-term use of sedatives and antidepressants before operation, alcoholism, drug dependence, etc.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| haemodynamics;The number of cases of limb movement that need to be dealt with during the operation;hypotension;respiratory depression; | — |
Countries
China
Contacts
Public ContactJia Shushan
Yantai Affiliated Hospital of Binzhou Medical College
Outcome results
None listed