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Study of transurethral resection of bladder tumor in one-piece using flexible cystoscope.

Study of transurethral resection of bladder tumor in one-piece using flexible cystoscope. - Study of transurethral resection of bladder tumor in one-piece using flexible cystoscope.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000045753
Enrollment
20
Registered
2021-10-20
Start date
2021-11-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Bladder tumor

Interventions

Tumour resection with a snare is performed on eligible patients.ESR biopsy, cold cup biopsy and TUR biopsy are performed in patients who meet the indicated criteria and for whom random biopsy is recom

Sponsors

University of Jikei Kashiwa hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) 20 years of age or older 2) ECOG Performance Status 0-2 3) No other active multiple cancers (including hematological malignancies). 4) The patient has been informed of the disease, and written consent for participation in this study with his or her own will. 5) Less than 10 mm transverse to the tumor base and less than 3 tumors in the bladder. 6) Suspected intermediate or high risk on preoperative examination and scheduled for random biopsy for diagnostic purposes. 7) Patients with positive urine cytology without intravesical tumors and scheduled for random biopsy for diagnostic purposes. Patients must meet all of the criteria in 1) to 4) and one of the criteria in 5) to 7) for enrollment.

Exclusion criteria

Exclusion criteria: 1) Patients with poorly controlled infections (including active tuberculosis). 2) Patients with serious complications (malignant hypertension, severe congestive heart failure, severe coronary insufficiency, myocardial infarction within 3 months, end-stage liver cirrhosis, poorly controlled diabetes, severe pulmonary fibrosis, active interstitial pneumonia, etc.). 3) Patients in an immunocompromised state due to disease or treatment. 4) Patients with severe mental disorders. 5) Patients who are participating in other clinical studies (including clinical trials). 6) Patients who are pregnant or lactating mothers. 7) Patients who are deemed unsuitable by the principal investigator or sub-investigator due to medical, psychological or other factors.

Design outcomes

Primary

MeasureTime frame
Pathological evaluation of ESRBT specimens

Secondary

MeasureTime frame
Adverse event rate, operative time, muscle layer sampling rate, degree of thermal degeneration or destruction of tissue

Countries

Japan

Contacts

Public ContactAkihiro Matsukawa

University of Jikei Kashiwa hospital Department of Urology

a.matsu.audi1055g@gmail.com04-7164-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026