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Calculi clinical trials

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NCT ID: NCT03559738 Completed - Ureteral Stones Clinical Trials

ESWL vs URS in Management of Upper Third Ureteric Calculi

Start date: June 1, 2016
Phase:
Study type: Observational

comparative study of two treatment modalities (ureteroscopy and extracorporeal shock wave lithotripsy) in management of upper third ureteral calculi

NCT ID: NCT03526458 Completed - Surgery Clinical Trials

Clinical Trial Evaluating the Efficiency of Holmium Laser Settings on Urinary Stones

Start date: July 30, 2019
Phase: N/A
Study type: Interventional

The primary objective of this study is to compare the time to acceptable stone fragmentation during clinical use of the holmium laser when using energy settings 0.2J vs 0.8J. The hypothesis is that holmium laser energy settings 0.8J will require less time than lower energy settings 0.2J for fragmenting urinary stones. The clinical practice is to treat urinary stones until the stone is reduced to fragments ≤ 2 mm in size. This is determined by using the laser fiber which is 273 microns to visually estimate the size of the resultant fragments as described by Patel et al, J Endo 2014. Investigators will standardize the effect of stone size by creating a ratio of stone size to treatment time. In this study, the frequency is set at 15Hz. Thus, the study contains two arms: 0.2J&15Hz, and 0.8J&15Hz. Patients will be randomized into the two groups by the ratio of 1:1.

NCT ID: NCT03503539 Completed - Kidney Stone Clinical Trials

Are the Stone Density and Location Useful Parameters for Small Kidney Stones?

Start date: April 2016
Phase: N/A
Study type: Interventional

The investigators aimed to evaluate whether these parameters could be guides for us in the selection of RIRS or Mini-PNL procedures in kidney stones that are smaller than 2 cm. The patients that have kidney stones smaller than two cm and be planned to undergo surgery were randomized into 2 groups prospectively. RIRS was performed in the RIRS group using a 7.5-F fiberoptic flexible ureterorenoscope while Mini-PCNL group was dilated up to 16.5F and mini-PCNL was performed with 12F nephroscopy. Preoperative characteristics, operative and postoperative results were compared in two groups. Thereafter, intra and intergroup comparisons were made to determine the effects of HU value, indicating the stone density, higher or less than 677 and the stone location on stone-free rates.

NCT ID: NCT03490383 Completed - Clinical trials for Microbial Colonization

Study of Microbiota in Bile From Patients With Common Bile Duct Stone During ERCP

Start date: February 16, 2018
Phase:
Study type: Observational [Patient Registry]

In this study, investigators will investigate the microbiota of bile in common bile duct stone participants. Three key questions are of concern. The first one is whether there is bacteriria in bile in participants without common bile duct stone. The second one is whether the microbiota of bile is similar with that of gut mucosa in common bile duct stone participants. The third one is whether the bacteria in bile of common bile participants with intact papillar is the same as that of participants underwent sphinctomy.

NCT ID: NCT03482375 Completed - Gall Stones Clinical Trials

Prospective Evaluation of Residual Bile Duct Stone by Peroral Cholangioscopy After Conventional ERCP

Start date: December 17, 2015
Phase:
Study type: Observational [Patient Registry]

Gallstone disease affects over 20 million Americans. Among patients with gallbladder disease, the prevalence of choledocholithiasis (stones in the bile duct) is estimated to be 10-20%. Endoscopic retrograde cholangiopancreatography (ERCP) is considered the standard of care for removing stones in the bile duct utilizing a variety of conventional methods including biliary sphincterotomy, sphincteroplasty, extraction balloon, retrieval basket, and mechanical lithotripsy. After removal of stones from the bile duct, an occlusion cholangiogram is usually performed to confirm complete bile duct clearance. However, cholangiogram can miss residual stones in 11- 30% of cases - especially in the setting of a dilated bile duct, large stones, severe pneumobilia, juxtapapillary diverticulum, primary sclerosing cholangitis, and after lithotripsy (mechanical, electrohydraulic, or laser). The approach to patients with choledocholithiasis requires careful attention because missed bile duct stones can cause recurrent biliary symptoms, pancreatitis, cholangitis, and has significant cost implication with the need for repeat imaging and/or procedures.

NCT ID: NCT03422042 Completed - Clinical trials for Common Bile Duct Calculi

Short Duration Versus Fourteen Days Antibiotic in Common Bile Duct Cholangitis

Start date: August 13, 2017
Phase: N/A
Study type: Interventional

Common bile duct stone cholangitis is a potentially fatal condition, characterized by an obstruction and bacterial infection of biliary system. The principles of management are appropriate biliary drainage and systemic antibiotics. There has been limited data about appropriate time of antibiotics in patient with successful endoscopic drainage.

NCT ID: NCT03421340 Completed - Biliary Stones Clinical Trials

Non-Complex Biliary Stones DSC vs ERC

Start date: September 21, 2018
Phase: N/A
Study type: Interventional

To prospectively compare non-complex biliary stone clearance using fluoroscopy/radiation-free direct solitary cholangioscopy (DSC) utilizing the SpyGlass™ system with non-complex biliary stone clearance using standard endoscopic retrograde cholangiography (ERC).

NCT ID: NCT03388060 Completed - Urologic Diseases Clinical Trials

(SWL) Versus (ODT) Versus Combined SWL And ODT For Radiolucent Stone

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

compare the efficacy of of ultrasound guided SWL versus dissolution therapy versus combined SWL and dissolution therapy in management of 1 - 2.5 cm renal stones.

NCT ID: NCT03344120 Completed - Pain Clinical Trials

Symptoms Comparison: Suture-stent vs Conventional Double-J Stents After Ureterorenoscopy. A Prospective Randomized Trial

Start date: January 8, 2020
Phase: N/A
Study type: Interventional

Double J ureteral stents (DJ) are widely used in urological practice and commonly inserted after most of ureteroscopies. Stent-related symptoms (SRS) represent a major issue. Many research lines have been explored with the aim of decreasing SRS: Vogt et al. projected a self-made pigtail suture stent (PSS) replacing the distal pigtail with a 0.3 Fr suture reaching the bladder, showing decreased SRS and good tolerance. To date, these promising results hasn't been confirmed by a prospective randomized controlled trial (RCT) involving a marketed PSS. Thus, we designed a prospective single-blind RCT to compare SRS caused by marketed PSS and conventional DJ after uncomplicated URS for stone treatment.

NCT ID: NCT03344107 Completed - Pain Clinical Trials

Stent-related Symptoms Comparison: Polaris Loop vs Vortek Double-J Stents

Start date: January 10, 2018
Phase: N/A
Study type: Interventional

Prospective randomized controlled single-blind parallel-group trial in order to compare symptoms related to loop-tail (Polaris Loop) stents versus conventional double J (Vortek) stents after uncomplicated flexible URS.