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INTRAOPERATIVE BLADDER INJURY ASSESSMENT IN TURBT USING BICEP

NCT07396038 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2026-02-09

No results posted yet for this study

Summary

Transurethral resection of bladder tumor (TURBT) is the cornerstone procedure in the diagnosis and treatment of bladder cancer but is associated with a spectrum of intraoperative bladder injuries ranging from minor mucosal tears to major perforations. Currently, there is no standardized intraoperative classification system specifically designed to grade and report these injuries during TURBT.

This study aims to apply the Bladder Injury Classification System for Endoscopic Procedures (BICEP) to TURBT in order to systematically classify intraoperative bladder injuries, evaluate their management, and explore their association with perioperative and early postoperative outcomes.

Conditions

  • Bladder (Urothelial, Transitional Cell) Cancer
  • TURBT
  • Bladder Injury

Interventions

OTHER

No intervention is assigned as part of this observational study. All procedures are performed as part of routine clinical care.

No intervention is assigned as part of this observational study. All procedures are performed as part of routine clinical care.

Sponsors & Collaborators

  • University Hospital Southampton NHS Foundation Trust

    collaborator OTHER

  • Medical University of Graz

    collaborator OTHER

  • Hannover Medical School

    collaborator OTHER

  • King's College London

    collaborator OTHER

  • Necmettin Erbakan University

    lead OTHER

Principal Investigators

  • Selçuk Güven, Prof · Necmettin Erbakan University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-15
Primary Completion
2026-12-30
Completion
2027-03-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07396038 on ClinicalTrials.gov