None listed
Conditions
Interventions
Medical Device : 1) Specific research methods
The aim is to evaluate the efficacy and safety of this medical device by applying it during surgical procedures.
Primary endpoint: Change in the degree o
Sponsors
Hallym University Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: - Patients who require urinary catheter insertion after surgery and are scheduled to undergo urinary catheter insertion - Patients with sufficient activity level to perform normal daily activities (Eastern Cooperative Oncology Group performance status of 0 or 1) - Patients who can read and consent to the informed consent form - Patients aged 19 to 80 years old
Exclusion criteria
Exclusion criteria: - Those who have undergone prior treatment for surgical diseases, such as radiation therapy, chemotherapy, or hormone therapy, before surgery, or those who are scheduled to undergo such treatment after surgery - History of previous surgery or radiation therapy in the pelvic cavity - Individuals with allergies to pain medication - Patients with severe hypertension - Pregnant women - Individuals who do not wish to participate in this study voluntarily - Individuals deemed unsuitable for participation in the clinical trial by the investigator's judgment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in the degree of urethral pain at 1 day after catheter insertion compared to before insertion | — |
Secondary
| Measure | Time frame |
|---|---|
| Degree of discomfort associated with the use of urinary catheters after surgery in each group;When removing the catheter from each patient, if the catheter is to be reused, indicate whether you want to use the same catheter or a different one.;Degree of urinary dysfunction symptoms before and after surgery for each group;Safety assessment | — |
Countries
Korea, Republic of
Contacts
Public ContactHWANIK KIM
Hallym University Medical Center
Outcome results
None listed