MedPath

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

Conditions
Ureteral Stricture
Registration Number
NCT04129645
Lead Sponsor
Peking University People's Hospital
Brief Summary

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

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
500
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 -

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Device related serious adverse eventsUp to 36 months

Number of device related serious adverse events

Patency rateUp to 36 months

Number of patients evaluated with hydronephrosis

Indwelling timeUp to 36 months

Number of months of the implant in the ureter

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Peiking university people's hospital

🇨🇳

Beijing, Beijing, China

© Copyright 2025. All Rights Reserved by MedPath