catheter-related bladder discomfort syndrome
Conditions
Interventions
Sponsors
The First Affiliated Hospital of Naval Medical University
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1. Planned to undergo elective urological endoscopic surgery; 2. Male patients; 3. Age 18–80 years; 4. Body mass index (BMI) 18–30 Kg/m^2; 5. American Society of Anesthesiologists (ASA) classification I–III; 6. Preoperative assessment indicates no difficult airway patients.
Exclusion criteria
Exclusion criteria: 1. Patients with severe dysfunction of vital organs; 2. High risk of reflux and aspiration; 3. Long-term users of sedative-hypnotics, narcotic analgesics, and antipsychotic drugs; 4. Patients who have taken sedative-hypnotics or narcotic analgesics within 1 day before surgery; 5. Known allergy to drugs used in the study; 6. Patients with psychiatric disorders, neurodegenerative diseases, or those unable to cooperate or communicate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Median Effective Dose of Oxycodone ;Median Effective Dose of Sufentanil; | — |
Secondary
| Measure | Time frame |
|---|---|
| Recovery time;score of catheter-related bladder discomfort ;Adverse reaction; | — |
Countries
China
Contacts
Public ContactYi Zhou
The First Affiliated Hospital of Naval Medical University
Outcome results
None listed