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Taking people in Hong KongPhase 1

Tests a flexible scope procedure to monitor upper tract urothelial carcinoma after surgery

Tests a flexible ureteroscopy under local anaesthesia in adults treated for upper tract urothelial carcinoma.

Plain-language title generated from the registry record
Registry title: Ambulatory Flexible URS for UTUC Surveillance

Key facts

Where
Hong Kong, Hong KongSee the 2 sites
Phase
Phase 1

Where in Hong Kong

  • Prince of Wales HospitalHong Kong, Hong KongTaking people
  • The Chinese University of Hong KongHong Kong, Hong KongNot yet recruiting

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
Chinese University of Hong Kong
Trial code
NCT06848868
Record updated
15 September 2025
Original description
This is a a prospective single-arm pilot study to investigate the safety and feasibility of flexible ureteroscopy under local anaesthesia. All consecutive patients who have undergone kidney-sparing surgery for managing upper tract urothelial carcinoma will be screened for study eligibility. The primary outcome is the procedural technical success rate. Secondary outcomes include the 30-day complication rate following flexible ureteroscopy, readmission rates, cost analysis, and patient-reported outcomes. Ureterorenoscopy will be conducted in the recruited patients under local anaesthesia in the ambulatory urology centre. Procedural details, technical success rates, adverse events and patient reported outcomes will be documented. The anticipated risks of this intervention are not expected to exceed those associated with the standard of care, that is ureterorenoscopy under anaesthesia. This pilot study aims to recruit a total of 10 subjects to assess the safety and feasibility of flexible ureterorenoscopy in an ambulatory care setting.Read full original descriptionShow less

Flexible Ureterorenoscopy for Surveillance of Upper Tract Urothelial Carcinoma-A Pilot Study

This is a a prospective single-arm pilot study to investigate the safety and feasibility of flexible ureteroscopy under local anaesthesia. All consecutive patients who have undergone kidney-sparing surgery for managing upper tract urothelial carcinoma will be screened for study eligibility. The primary outcome is the procedural technical success rate. Secondary outcomes include the 30-day complication rate following flexible ureteroscopy, readmission rates, cost analysis, and patient-reported outcomes. Ureterorenoscopy will be conducted in the recruited patients under local anaesthesia in the ambulatory urology centre. Procedural details, technical success rates, adverse events and patient reported outcomes will be documented. The anticipated risks of this intervention are not expected to exceed those associated with the standard of care, that is ureterorenoscopy under anaesthesia. This pilot study aims to recruit a total of 10 subjects to assess the safety and feasibility of flexible ureterorenoscopy in an ambulatory care setting.

Inclusion: Aged 18 years or older; Capable of giving informed consent; Having undergone an kidney-sparing surgery (endoscopic operation or segmental ureterectomy).

Exclusion: Allergy to transurethral lidocaine jelly; On anticoagulation or anti-platelet medication with contraindications for cessation prior to the procedure; Structural abnormalities in the upper urinary tract on the intended side of examination.

ClinicalTrials.gov NCT06848868