cervical cancer
Conditions
Interventions
Control Group:Bilateral paracervical nerve block was not performed
Group:Bilateral paracervical nerve block was performed
Sponsors
The Fourth Hospital of Hebei Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: ASA ? - ? level;Patients receiving painless post-implantation therapy for cervical cancer;Aged 18-75 years;They agreed to participate in the study and signed the informed consent form
Exclusion criteria
Exclusion criteria: Puncture site infection;Allergic to experimental drugs.Patients with mental illness or unable to cooperate with the operation;Severe hepatic and renal failure or heart failure (New York College of Cardiology grade III or higher);
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS score;Incidence of hypoxemia;WHO Pain scale;Nausea and vomiting occur;Physical activity condition;the satisfaction of patients;Surgeon satisfaction; | — |
Secondary
| Measure | Time frame |
|---|---|
| Circulatory adverse events;heart rate;mean arterial pressure;operative time; | — |
Countries
China
Contacts
Public ContactJianfeng Fu
The Fourth Hospital of Hebei Medical University
Outcome results
None listed