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Safety and Efficacy of URS Stents in the Treatment of Ureteral Stricture

P

Peking University

Status

Enrolling

Conditions

Ureteral Stricture

Treatments

Device: URS

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

A prospective observational study aimed to assess the efficacy and safety of Allium ureteral stent long-term indwelling in the treatment of ureteral stricture.

Enrollment

500 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Benign diseases: UPJ, ischemic injury caused by surgical separation, endoscopic surgery injury, heat injury by laser lithotripsy, infection (chronic inflammation, tuberculosis), peri-ureteral fibrosis caused by endometriosis, ureteral anastomotic stenosis after renal transplantation, ureteral fistula, multiple polyps;
  2. Malignant diseases: ureteral anastomotic stricture after urinary diversion, stricture caused by compression of abdominal and/or pelvic tumors, stricture caused by urinary tract tumors, stricture caused by radiotherapy for colon or cervical cancer, ureteral fistula

Exclusion criteria

  1. Combine with hypertonic neurogenic bladder (except for patients with long-term indwelling catheter)
  2. Colon resection surgery patients -

Trial contacts and locations

1

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Central trial contact

Weihong Feng

Data sourced from clinicaltrials.gov

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