Skip to content

Researcher clinical trial to evaluate the satisfaction of experimenters and subjects with using deep body wound epithelial tissue using urethral catheter to prevent urethral stenosis after bladder tumor resection (TURB) through the urethra

A multicenter, randomized, single-blind, investigator clinical trial to evaluate the satisfaction of using deep body wound epithelial tissue using a urethral catheter for the prevention of urethral stenosis after transurethral bladder tumor resection.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0007010
Enrollment
198
Registered
2022-02-18
Start date
2022-02-11
Completion date
Unknown
Last updated
2022-05-30

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 : Test group: group injecting deep body cavity wound dressings into the urethra using a urethral catheter After surgery, using the urethral catheter for clinical trials, the drug is in

Sponsors

Asan Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Patients scheduled to undergo transurethral bladder tumor removal,aged >=18 and <80 years

Exclusion criteria

Exclusion criteria: 1) Patients who have participated in other clinical trials within 1 month prior to being registered for clinical trial and have received drug administration or medical device treatment 2) Those with congenital abnormalities in the urinary or reproductive system 3) If you have neurogenic bladder disease 4) If you have had a previous radical prostatectomy for prostate cancer 5) Those with a history of allergy or hypersensitivity to substances and catheter used to prevent urethral strictures 6) There is dermatitis in catheterization 7) People with immunodeficiency diseases (eg, HIV-infected) 8) People with blood clotting disorders 9) A person who is inappropriate to participate in a clinical trial because the investigator judges it to be other ethically or because it may affect the clinical trial results

Design outcomes

Primary

MeasureTime frame
user convenience (Likert Scale Degree of Satisfaction Questionnaire)

Secondary

MeasureTime frame
Visual analog scale (VAS) ; operator's convenience (Likert Scale);Evaluating the rate of urethral stricture through cystourethral endoscopy

Countries

Korea, Republic of

Contacts

Public ContactDalsan You

Asan Medical Center

dalsanyou@amc.seoul.kr+82-2-3010-3979

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 6, 2026