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The efficacy of regular lidocaine gel delivery via 4-way Foley catheter for postoperative catheter-related urethral pain in male patients undergoing transurethral resection of the bladder tumor

The efficacy of regular lidocaine gel delivery via 4-way Foley catheter for postoperative catheter-related urethral pain in male patients undergoing transurethral resection of the bladder tumor : Randomized, controlled, open, comparative intervention study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0008737
Enrollment
100
Registered
2023-08-25
Start date
2022-12-05
Completion date
Unknown
Last updated
2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : 1) Perform general transurethral bladder tumor resection after general anesthesia for clinical research subjects who have given prior consent 2) After performing transurethral bladder

Sponsors

Seoul Metropolitan Government Seoul National University Boramae Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1)A male subject to transurethral cystectomy under general anesthesia after being hospitalized for a tumor in the bladder among patients suspected of having bladder cancer through radiological examinations such as computed tomography and ultrasound and examinations such as cystoscopy 2)Those who are 18 years of age or older at the time of writing the consent form. 3)Those who can read and understand the consent form and have a willingness to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Those who refused to participate in this study 2. Those who have difficulty understanding the consent form due to suspected cognitive impairment 3. Persons with a history of kidney transplant or urinary tract diversion 4. Those with a history of trauma to the pelvis or urinary tract 5. A drug or alcohol addict 6. Those who have received clinical trial drugs within 3 months before screening 7. Test laboratory staff and their families directly involved in the conduct of the test 8. Patients who need continuous pain medication administration for reasons other than transurethral cystectomy during the postoperative urinary catheterization period 9. Person with psychiatric disorder 10. In case bacteriuria of 10^5 or more is observed in the preoperative examination

Design outcomes

Primary

MeasureTime frame
Efficacy(Vas,Likertscale)

Secondary

MeasureTime frame
Drug side effects, Adverse event

Countries

Korea, Republic of

Contacts

Public ContactKKOTNIM PARK

Inje University Haeundae Paik Hospital

qazwsx9@nate.com+82-51-797-0344

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026