Postoperative pain
Conditions
Interventions
Experimental group:Oxycodone for pain relief
Control group:Fentanyl for pain relief
Sponsors
Qilu Hospital of Shandong University
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Patients aged >=18 years who underwent elective laparoscopic hysteromyectomy for uterine fibroids in Qilu Hospital; 2.ASA I-II level; 3.The patient provides written informed consent; 4.The patient can cooperate to obtain the result measurement; 5.The patient agrees to participate.
Exclusion criteria
Exclusion criteria: 1.Patients who are pregnant or breastfeeding; 2.The patient suffers from dementia or severe mental illness; 3.The patient has a history of oxycodone allergy; 4.Patients with respiratory depression, paralytic ileus, etc. who should not use oxycodone hydrochloride; 5.Patients who have performed additional surgical operations or abandoned the original surgical arrangement; 6.The patient is participating in other clinical trials; is taking opioids and/or antidepressants; 7.Patients with BMI>=30.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Ramsay sedation score;Self-rating depression scale; | — |
Countries
China
Contacts
Public ContactDong Ping
Qilu Hospital of Shandong University
Outcome results
None listed