Womb-related diseases in women
Conditions
Interventions
Intervention group:Intravenous lidocaine and propofol combined with paracervical block
Sponsors
The Cixi People's Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1.Female patients scheduled for elective hysteroscopic surgery; 2.ASA physical status I–II; 3.Age 18–65 years; 4.Body mass index (BMI) >= 18 and <= 30 kg/m^2; 5.Voluntary participation with informed consent to join this study;
Exclusion criteria
Exclusion criteria: 1.Pregnant or lactating patients; 2.Patients who refuse to provide informed consent; 3.Use of psychotropic drugs or presence of psychiatric disorders; 4.Severe cardiopulmonary disease; 5.Morbid obesity (BMI > 30 kg/m^2); 6.Known allergy to lidocaine or propofol; 7.Severe hepatic or renal dysfunction; 8.High risk of obstructive sleep apnea; 9.Patients with an anticipated difficult airway;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Protocol success rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative complications;QoR-15 score ;Operation type and operation, anesthesia time, awake time;Pain score;Patient and surgeon satisfaction;Propofol injection pain during induction;Last incidence;Postoperative malignant vomiting; | — |
Countries
China
Contacts
Public ContactJiliang He
The Cixi People's Hospital
Outcome results
None listed