Kidney Stones Clinical Trial
Official title:
Multicentred, Randomized Control Trial Comparing Narrow Versus Wide Focal Zones for Shock Wave Lithotripsy of Renal Calculi
Verified date | October 2017 |
Source | St. Michael's Hospital, Toronto |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Shockwave lithotripsy (SWL) is a safe, non-invasive treatment for renal calculi. During SWL energy is focused on in order to break kidney stones and this energy can be varied in size from a narrow (or small) focal zone to a wide (or large) focal zone. This is a multi-centered, randomized study comparing the single treatment success rates of narrow and wide focal zones during SWL.
Status | Completed |
Enrollment | 275 |
Est. completion date | April 2017 |
Est. primary completion date | November 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Stone must be radiopaque on a KUB (kidney, ureter and bladder) radiograph, and located within the renal collecting system. - Patients must have had a CT scan within the past 30 days. - Stones must be solitary, between 5 and 15 mm in maximal diameter. - Patient must consent to the trial and be willing to return to their respective lithotripsy unit at 2 weeks and 3 months for follow-up. - Patients must be treated on the Storz Modulith SLX-F2 machine Exclusion Criteria: - More than one renal calculus on the treated side. - Radiolucent stones (uric acid, indinavir) or cystine stones. - Stone size < 5 mm and > 15 mm. - Previous surgical intervention on upper tracts within past five years. - Congenital anatomic anomalies of the kidney, ureters or bladder (such as calyceal diverticulum, horseshoe kidney, etc.) - Patient currently taking an a-blocker (alfuzosin, terazosin, doxazosin, tamsulosin, prazosin), calcium channel blocker (verapamil, diltiazem, nifedipine, nicardipine, bepridil, mibefradil), or corticosteroids. - Pregnancy. - Age < 18 years. - Active urinary tract infection. - Patient exceed weight limit for SWL table (>500 lbs) - Previous SWL treatment for this stone. - Uncorrected coagulopathy |
Country | Name | City | State |
---|---|---|---|
Canada | St. Joseph's Hospital, University of Western Ontario | London | Ontario |
Canada | St. Michael's Hospital, University of Toronto, Toronto, Lithotripsy suite, 5th floor Cardinal Carter North Wing | Toronto | Ontario |
Canada | Vancouver General Hospital, Jim Pattison Pavilion G floor station 5 GI/GU Lithotripsy suite | Vancouver | British Columbia |
Lead Sponsor | Collaborator |
---|---|
St. Michael's Hospital, Toronto | University of British Columbia, University of Toronto, University of Western Ontario, Canada |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | SWL efficiency quotient comparison between narrow focus vs wide focus | Comparison of single-treatment lithotripsy success rates at 2 and 12 weeks post-lithotripsy. Successful treatment will be defined as either stone-free status or presence of clinically insignificant asymptomatic residual fragments = 4 mm. SWL efficiency quotient for the treatment groups, as calculated by the standardized formula: % stone-free divided by (100 + % re-treated + % auxiliary procedures). | 2 and 12 weeks | |
Secondary | Incidence of perirenal hematomas | Comparing the narrow and wide foci for the presence of perirenal hematomas post treatment on ultrasound. | post treatment | |
Secondary | Biomarkers for renal injury | Comparisons of urinary markers for identifying renal injury | day 0; day 1; 1 week | |
Secondary | Time to stone passage | Time it took to pass the stone for both arms will be compared for the 3 month follow up time. | 12 weeks | |
Secondary | Pain will be compared between narrow vs wide focus arms | Visual analog pain scores will be compared between arms. | day 0 (post treatment) | |
Secondary | Complication rates | Complication rates will be compared between narrow and wide focus treatment arms. | 12 weeks |
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