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Calculi clinical trials

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NCT ID: NCT01604304 Completed - Clinical trials for Extracorporeal Shockwave Lithotripsy, Flexible Ureteroscopy

Flexible urétéroscopy Versus Extracorporeal Shockwave Lithotripsy in Renal Calculi

CALIX-1
Start date: May 2012
Phase: N/A
Study type: Interventional

Flexible ureteroscopy is a recent procedure to treat renal stone. Extracorporeal shockwave lithotripsy was the gold standard treatment for calculi between 5 and 20 mm. In literature, the two procedures are available to treat these stones with a good stone free rate. There is no prospective randomized study comparing these two treatments. Our study will define with a good level of evidence which technique is the best with regard to the stone free rate, secondary procedure rate and adverse effect.

NCT ID: NCT01589484 Completed - Urolithiasis Clinical Trials

Impact of Renal Anatomy on Shock Wave Lithotripsy Outcomes for Lower Pole Kidney Stones

Start date: April 2012
Phase: N/A
Study type: Interventional

Kidney stone disease affects almost 10% of overall population, often requiring a surgical intervention. Currently, shock wave lithotripsy is considered a first-line treatment option for patients suffering from symptomatic kidney stones smaller than 2.0 cm, providing reasonable stone-free rate. Actually, the outcomes from SWL vary largely due to several factors including stone burden, stone density, stone-skin distance (SSD), and patient's body habitus. Furthermore, the imaging exam modality (i.e. ultrasound versus computed tomography scan) performed to assess the presence of residual fragments also impacts on SWL outcome analysis. We aim to perform a well-controlled prospective evaluation of all variables that may impact on fragmentation and clearance of lower pole calculi after SWL. These variables are assessed exclusively by a noncontrast computed tomography scan (NCCT), eliminating the necessity of an intravenous urography to study renal collecting system anatomy; an imaging exam that is not routinely performed anymore for kidney stone patients.

NCT ID: NCT01571271 Completed - Gall Stones Clinical Trials

Electrohydraulic Versus Laser Lithotripsy for Treatment of Difficult to Remove Biliary Stones

EHLvlaser
Start date: January 2010
Phase: N/A
Study type: Interventional

Bile duct stones that can't be removed by conventional means can often be removed after fragmentation by shock waves (lithotripsy). The shock waves that are used for fragmentation of these stones are generated by electric sparks (electrohydraulic lithotripsy) or laser (laser lithotripsy). Although both techniques have been used for many years, there are no studies comparing the efficacy of the two. The purpose of this study is to find out which technique is more effective.

NCT ID: NCT01539265 Completed - Urinary Calculus Clinical Trials

A Dose-finding Study of Silodosin in Patients With Urinary Calculi

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and the safety of silodosin in urinary calculi patients.

NCT ID: NCT01525355 Completed - Calculi Clinical Trials

EUS Prior to ERCP in the Positive Setting of Positive Intraoperative Cholangiogram (IOC) During Cholecystectomy

Start date: October 2010
Phase: N/A
Study type: Observational

Performing an EUS prior to ERCP in the setting of a positive intraoperative cholangiogram will identify and risk stratify patients for the presence of CBD stones and strictures.

NCT ID: NCT01450566 Recruiting - Renal Calculi Clinical Trials

Intraureteral Lidocaine for Post-Ureteroscopy Pain

Start date: September 2011
Phase: N/A
Study type: Interventional

Ureteroscopy (URS) is minimally invasive procedure for management of renal stones. URS is often involves concomitant of an indwelling ureteral stents. Placements of these stents include pain, bladder irritability, infection, migration, encrustation and stones. Pain is one of most significant problem of ureteral stents. There are no satisfactory measures to deal with this problem. A novel approach to manage the pain is to load a drug onto ureteral stent and deliver the drug into the urinary tract at controlled release rate. Lidocaine has been proven to be effective for management of the pain associated with interstitial cystitis. This agent has the potential for management of post-URS pain.

NCT ID: NCT01443702 Completed - Kidney Calculi Clinical Trials

Use of Lapis Judaicus to Dissolve Kidney Stones

Start date: January 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The investigators will investigate the safety and effectiveness of an Iranian traditional medicine regarding its ability to dissolve existing kidney stones. Calcium stone formers will be recruited for a 12 week trial. Each subject will receive Lapis judaicus or placebo in random order. End points are changes in urinary chemistries and stone burden by Ultra sonography / CT scan. It will be used in proven calcium stone forming adults who are not pregnant. This phase is a double blind, randomized, placebo controlled Entry, first and 12 week 24 hour urine supersaturations, pH and sodium determinations will be collected. Entry and final stone quantification Ultra sonography / CT scan will be performed. End points will be changes in urine chemistry/supersaturation and stone quantitative stone volume.

NCT ID: NCT01437904 Completed - Renal Calculi Clinical Trials

A Pilot Study Assessing The Feasibility Of Outpatient Tubeless Percutaneous Nephrolithotomy (PCNL)

Start date: March 2011
Phase: N/A
Study type: Interventional

Outpatient tubeless Percutaneous nephrolithotomy (PCNL) could potentially improve patient care and result in significant cost savings for our hospital each year. If this pilot study is successful, Queen's/KGH will lead a collaborative national multicentre trial to further establish the role of this new approach in the surgical treatment of kidney stones.

NCT ID: NCT01420354 Terminated - Kidney Stones Clinical Trials

Can a Spot Urine Replace or Improve 24 Hour Urine Collections in Kidney Stone Patients

Start date: August 2009
Phase: N/A
Study type: Observational

This study will sought to determine if limited urine collections can provide similar or more informative data than standard 24-hour urine collections used to evaluate kidney stone formers.

NCT ID: NCT01355341 Unknown status - RENAL CALCULI Clinical Trials

Safety and Efficacy of Herbmed Plus in Patients withRenal Calculi

HerbmedPlus
Start date: April 2010
Phase: Phase 2
Study type: Interventional

More specifically, the present invention relates to a 'Herbal Preparation' that is useful for - Treatment of Renal calculi - Reduction in the stone size & surface area - The expulsion of stone - Decreased need of Analgesic(Antiinflammatory Effect) - Stops the recurrence and reformation of renal