Patients undergoing laparoscopic total hysterectomy
Conditions
Interventions
Experimental group:hydromorphine treatment
Control group:Sevoflurane relies on inhalation anesthesia
Sponsors
Department of Anesthesiology, Tianjin Nankai Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Women aged 30-65 yearsweighed 40-70kg with ASA status I or II, scheduled for elective laparoscopic total hysterectomy of<3h duration at Tianjin Nankai hospital between June 2017 and March 2018 were enrolled in this study. All patients have no history of chronic pain, mental illness, and a long-term history of pain reliever.
Exclusion criteria
Exclusion criteria: Exclusion criteria included cardiovascular disease (hypertension, arrhythmia or myocardial ischaemia), haemodynamic instability (active bleeding, hypovolaemia or loss of body fluid), asthma or chronic obstructive pulmonary disease, allergy to the study drug and body mass index 30 kg/m2.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cdyn;RI; | — |
Countries
China
Contacts
Public ContactYu Jianbo
Department of Anesthesiology, Tianjin Nankai Hospital
Outcome results
None listed