Stent Related Symptoms Defined by Ureteral Stent Symptom Questionnaire in Patients With Image-Informed Ureteral Stent Lengths

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorWeill Medical College of Cornell University

About this trial

Placement of a ureteral stent at the end of ureteroscopy is commonly performed in endourology. The purpose of this study is to determine whether ureteral stents whose lengths are calibrated to a participant's specific ureteral length based on imaging are better tolerated than one-size-fits-all variable length ureteral stents. The investigators hypothesize that ureteral stent lengths calibrated to the ureteral length of each participant will be better tolerated.

Eligibility criteria

Qualifiers

Male or female age 18-80 years

Urolithiasis requiring ureteroscopic management with ureteral stent placement

CT scan showing evidence of upper tract urolithiasis

Negative pre-operative urine culture

Disqualifiers

Known urinary tract anatomical abnormality, reconstructed urinary system, or congenital anomaly

Ureteral stent inserted within the last 31 days

History of peptic ulcer disease, symptomatic benign prostatic hyperplasia, interstitial cystitis, chronic pelvic pain syndrome, neurogenic lower urinary tract dysfunction, ureteral stricture disease

Chronic narcotic use

Trial design

Treatments tested in this trial

  • Variable length ureteral stent
  • Image-informed length ureteral stent

Treatment groups

128 Participants
are divided into 2 treatment groups