None listed
Conditions
Interventions
Medical Device : To evaluate the efficacy and safety of eluting analgesics into the urethra through a urethral catheter compared to injecting normal saline through a urethral catheter after urologic s
Sponsors
Hallym University Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: - Patients scheduled to undergo catheterization due to the need for catheterization after urologic surgery - Active enough to perform normal activities of daily living (Eastern Cooperative Oncology Group performance status of 0 or 1) - Patients able to read and give informed consent - At least 19 years of age and less than 80 years of age
Exclusion criteria
Exclusion criteria: - Prior treatment for urinary system disease, such as radiation therapy, chemotherapy, or hormonal therapy prior to surgery or planned after surgery - Previous surgery or radiation therapy in the pelvic cavity - Allergic to pain medications - Patients with severe hypertension - Are pregnant - Do not want to participate in this study voluntarily - Anyone who, in the opinion of the investigator, is unsuitable for participation in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in urethral pain level from pre-catheterization to 1 day post-catheterization | — |
Secondary
| Measure | Time frame |
|---|---|
| Level of discomfort with the use of postoperative analgesic eluting catheters in each group;For each group, the extent to which, at the time of catheter removal, if the catheter were to be reused in the future, they would prefer to use analgesic eluting catheter rather than a generic one.;Level of lower urinary tract symptoms before and after surgery in each group | — |
Countries
Korea, Republic of
Contacts
Public ContactHwanik Kim
Hallym University Medical Center
Outcome results
None listed