RECRUITINGINTERVENTIONAL
Tandem Polyurethane Stents Compared to Single Silicone Stent for Malignant Ureteral Obstruction
About This Trial
Malignant ureteral obstruction (MUO) is an extrinsic ureteral obstruction caused by malignant diseases. This study aim to compare tandem 6 Fr Percuflex™ stents and single large-caliber 8Fr silicone stent in patients with MUO. The primary endpoint is stent failure rate. The secondary endpoints are patient comfort, quality of life and overall survival.
Who May Be Eligible (Plain English)
Who May Qualify:
- patient with malignant ureteral obstruction
Who Should NOT Join This Trial:
- ureteral obstruction of other causes
- Language comprehension or other limitation in giving willing to sign a consent form
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* patient with malignant ureteral obstruction
Exclusion Criteria:
* ureteral obstruction of other causes
* Language comprehension or other limitation in giving informed consent
Treatments Being Tested
DEVICE
ureteral stent\s insertion
ureteral stent\\s insertion in the operating room
Locations (2)
Rabin Medical Center
Petah Tikva, Israel
Sheba medical center
Ramat Gan, Israel