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Clinical Trials/NCT03855787
NCT03855787
Completed
Not Applicable

Ureteral Stent Placement After Ureteroscopy for Renal Stones: A Randomized Controlled Trial

Vanderbilt University Medical Center7 sites in 2 countries103 target enrollmentNovember 11, 2019
ConditionsKidney Calculi

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Kidney Calculi
Sponsor
Vanderbilt University Medical Center
Enrollment
103
Locations
7
Primary Endpoint
Total number of complications
Status
Completed
Last Updated
last year

Overview

Brief Summary

The rationale for this study is to determine if there is a difference in complications among patients undergoing ureteroscopy for renal stones who receive a stent compared to not receiving a stent postoperatively.

Detailed Description

Kidney stones affect 9% individuals within the United States, and the prevalence is increasing. Over the last few decades, ureteroscopy has become the most commonly performed stone procedure. However the complication rate after ureteroscopy is not insignificant. Reducing morbidity after ureteroscopy would improve patient outcomes and reduce health care utilization. A major contributor to patient morbidity after ureteroscopy is the ureteral stent, which is placed at the time of surgery and left in place 1-2 weeks after surgery. The rationale for utilizing stents is to prevent urinary obstruction from edema or stone fragments. On the other hand, stents cause hematuria, pain, and lower urinary tract symptoms. Additionally, stent-related symptoms are often misdiagnosed as urinary tract infections leading to unnecessary antibiotic use. The clinical utility of ureteral stents after ureteroscopy has not been well studied, specifically a stone located in the kidney. Prior studies on stent-less ureteroscopic procedures have focused on treatment of ureteral stones and not stones located in the kidney, have had restrictive inclusion and exclusion criteria, are primarily from single center institutions, and most being performed \~15 years ago. Surgical techniques and device innovations have changed the procedure since that time. To date, there have been only 2 studies that included stone located in the kidney showing no difference in unplanned hospital revisits, however both combined analyses with ureteral stones and selection bias was an issue for both studies. In addition, there is a lack of studies assessing opiate use, impact of quality of life with stent placement, and loss of work related to stent placement

Registry
clinicaltrials.gov
Start Date
November 11, 2019
End Date
January 1, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ryan Hsi

Associate Professor

Vanderbilt University Medical Center

Eligibility Criteria

Inclusion Criteria

  • nonobstructing renal stone 1.5cm total stone diameter (if multiple stones, then sum of maximum diameters) or less undergoing ureteroscopy

Exclusion Criteria

  • age \< 18 years
  • pregnancy status
  • ureteral stone
  • preoperative hydronephrosis
  • indwelling nephrostomy tube
  • planning bilateral ureteroscopy or subsequent staged ureteroscopy
  • solitary kidney or eGFR \<60 mL/min (CKD stage 3 or greater)
  • variant anatomy including horseshoe kidney, pelvic kidney, prior urinary tract reconstruction

Outcomes

Primary Outcomes

Total number of complications

Time Frame: 30 days after ureteroscopy

Total number of complications - Defined as ER visits related to procedure, unanticipated provider visit, and hospitalization

Secondary Outcomes

  • % return to work(5-10 days after ureteroscopy)
  • WISQOL (Wisconsin Stone Quality of Life Questionnaire)(baseline to 5-10 days after ureteroscopy)
  • Cumulative opiate morphine equivalent dosing (MED)(baseline to 5-10 days after ureteroscopy)
  • PROMIS (Patient-Reported Outcomes Measurement Information System) form 6a(baseline to 5-10 days after ureteroscopy)
  • Number of participants with abnormal imaging findings(4-8 weeks after ureteroscopy)
  • Number of participants with symptomatic urinary tract infection (UTI)(Baseline 5-10 days after ureteroscopy)

Study Sites (7)

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