ClinicalTrials.Veeva

Menu

A Study of Balloon Dilatation for the Treatment of Benign Ureteral Stricture

N

Naval Military Medical University

Status

Unknown

Conditions

Stricture Ureter

Treatments

Device: balloon dilatation

Study type

Observational

Funder types

Other

Identifiers

NCT04021901
SHOT-20181112

Details and patient eligibility

About

This study is designed to treat benign ureteral stricture with balloon dilatation through prospective multicenter studies. It aims to indications, procedure standards, and therapeutic effects of balloon dilation, and provide further guidance for endoscopic treatment of benign ureteral stricture.

Full description

Benign ureteral stricture refers to a urinary tract obstruction caused by a partial or full ureteral lumen that is less normal than normal. It can lead to urinary dilatation, water accumulation, and renal colic in the upper segment of the stenosis. If treat not in time, it will affect renal function and even causes irreversible kidney failure.In recent years, with the development of endoscopic techniques, it provides a cost-effective and less invasive treatment for the treatment of ureteral stricture. In recent years, with the development of endoscopic techniques, it has provided a cost-effective and less invasive treatment for the treatment of ureteral stricture, and has achieved satisfactory results. Therefore, more and more urologists choose to treat ureteral stricture under endoscopy. The techniques of urinary endoscopic treatment of benign ureteral stricture include ureteral balloon dilatation, ureteral holmium laser incision, and ureteral stent implantation. Among them, the ureteral balloon dilatation technique is characterized by the use of a balloon to uniformly force the ureteral wall, tearing the narrow scar tissue, expanding the inner diameter of the ureter, recanalizing the urinary tract, and alleviating hydronephrosis. It have been reported with less complications and simple procedure. However, there's still no consensus on its treatment indication,procedure standards and curative effect. This study is designed to treat benign ureteral stricture with balloon dilatation through prospective multicenter studies. It aims to indications, procedure standards, and therapeutic effects of balloon dilation, and provide further guidance for endoscopic treatment of benign ureteral stricture.

Enrollment

420 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • • Subject has provided informed consent and indicated a willingness to comply with study treatments

    • Subject is 18-70 yrs of age
    • Subject can be either male or female
    • Subject diagnosed with ureteral stricture or atresia by enhanced CTU, intravenous pyelography or retrograde pyelography;
    • Subject's ureteral stenosis length is ≤ 2cm (single or multiple segments)

Exclusion criteria

  • • Subject has any congenital ureteral anatomical deformity, abdominal organ compression, oppression caused by malignant tumor metastasis

    • Subject has poor result after endoscopic balloon dilatation treatment
    • Subject has a GFR <25% on the affected side of the kidney
    • Subject has an active urinary tract infection (e.g., cystitis, prostatitis, urethritis, etc.)
    • Subject has been diagnosed with a urethral stricture or bladder neck contracture
    • Subject has been diagnosed with a urinary tract infection related to stone obstruction within two weeks
    • Subject has severe hematuria that might blur the vision of the endoscopy
    • Subject is pregnant or in monthly period
    • Subject has coexistent disease like systemic disease, heart disease, lung disfuction or other diseases that could not tolerate the endoscopic surgery or anesthesia.
    • Subject has unadjusted diabetes or high blood pressure
    • Subject has a disorder of the coagulation cascade system that would put the subject at risk for intraoperative or postoperative bleeding
    • Subject is unable to discontinue anticoagulant and antiplatelet therapy preoperatively (2 weeks)

Trial design

420 participants in 2 patient groups

F21
Description:
balloon diameter F21
Treatment:
Device: balloon dilatation
F24
Description:
balloon diameter F24
Treatment:
Device: balloon dilatation

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems