Catheter related bladder discomfort (CRBD)
Conditions
Interventions
Compound lidocaine cream group:none
Postoperative lidocaine group:none
Control group:none
Sponsors
The Third Affiliated Hospital Sun Yat-sen University
Eligibility
Sex/Gender
All
Age
18 Years to 120 Years
Inclusion criteria
Inclusion criteria: Patients over 18 years old, underwent endotracheal intubation general anesthesia, urinary catheterization after anesthesia induction, ASA I-II, from January 1, 2023 to March 31, 2024;
Exclusion criteria
Exclusion criteria: 1.Patients who did not complete the catheter related bladder discomfort (CRBD) score; 2.Patients with prostatic hyperplasia, urethral stricture, urethral injury, overactive bladder, nervous bladder, etc; 3.Patients who were allergic to any of the drugs used in the study; 4.Patients with severe cardiopulmonary dysfunction, severe hepatorenal insufficiency, severe diabetes; 5.Patients with cognitive impairment, mental disability, or with history of mental illness, long-term use of analgesics or sedatives; 6.Patients participating in other clinical studies at the same time;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| CRBD score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain NRS score;Vital signs; | — |
Countries
China
Contacts
Public ContactJingru Pan
The Third Affiliated Hospital Sun Yat-sen University
Outcome results
None listed