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Renal Stone clinical trials

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NCT ID: NCT04695951 Completed - Urolithiasis Clinical Trials

Efficacy and Safety of Renalof® in the Removal of Calculi Smaller Than 10 mm Located in the Reno-Ureteral Tract

Start date: August 1, 2019
Phase: Phase 2
Study type: Interventional

Given the high recurrence of urolithiasis in patients, the search for less aggressive and preventive treatments is increasingly necessary. Renalof® is presented as an alternative to herbal medicine being a product that, due to its diuretic and demineralization properties of kidney stones, has been widely used in this patient population, disintegrating and eliminating calcium oxalate and struvite stones in a painless in the genitourinary system. With the objective of determining the efficacy of this therapy, an observational, prospective, randomized, single-blind, two-arm study was carried out: treatment group with Renalof® and control group, placebo.

NCT ID: NCT04404855 Completed - Kidney Stone Clinical Trials

Antibiotic Selection Using Next Generation Sequencing vs Urine Culture

ACCESS
Start date: December 18, 2019
Phase: N/A
Study type: Interventional

This is a randomized controlled clinical study evaluating the use of next-generation sequencing (NGS) to improve antibiotic prescribing before ureteroscopy or percutaneous nephrolithotomy.

NCT ID: NCT04346134 Completed - Renal Stone Clinical Trials

Mini- Percutaneous Nephrolithotomy Versus Extracorporeal Shock Wave Lithotripsy for High Density Renal Stones

Start date: July 14, 2020
Phase: N/A
Study type: Interventional

Several studies were conducted to compare extracorporeal shockwave lithotripsy (SWL) and percutaneous nephrolithotomy (PNL) as treatment options for medium size lower caliceal high dense stones. However, no studies compared these options for non- lower polar stones. In the present study the investigators will compare mini-PNL and SWL in treatment of non- lower polar, medium size, high dense renal stones in reference to the stone free rate and safety of the procedures. Pre-operative evaluation including abdominal non-contrasted computed tomography will be performed for all patients. Patients will be randomly allocated into two equal groups and will be treated by either mini-PNL or SWL. postoperative, patients will be followed by regularly for 3 months. the outcome of the procedures will be evaluated and compared between groups.

NCT ID: NCT04160936 Completed - Renal Stone Clinical Trials

The Efficacy of Peritubal Analgesic Infiltration in Postoperative Pain Following Percutaneous Nephrolithotomy

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

The investigators aim to investigate the effect of peritubal local anesthetic infiltration on pain scores and analgesic consumption in patients who underwent percutaneous nephrolithotomy.

NCT ID: NCT04077359 Completed - Clinical trials for Renal Cell Carcinoma

Prospective Trial for Examining Hematuria Using Computed Tomography

PROTEHCT
Start date: September 15, 2019
Phase: N/A
Study type: Interventional

The primary objective is to evaluate whether one-phase nephrographic CT (experimental) is sufficient to detect urothelial cell carcinoma in patients with hematuria compared to the traditional four-phase CT (control).

NCT ID: NCT03828175 Completed - Renal Stone Clinical Trials

Basic Hemodynamic Monitoring Reliability During Percutaneous Nephrolithotomy.

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

This prospective pre and post-quasi-descriptive single group interventional study will be done at urology and nephrology center -Mansoura University during the year 2019, for a 3-month duration, starting 1-2-2019 till 1-4-2019 after approval of IRB (Institutional Review Board) code no R/18.03.103 on 5/5/2018, Mansoura Faculty of Medicine. correlating Basic hemodynamics with noninvasive cardiac output for diagnostic reliability during percutaneous nephrolithotomy hidden bleeding under spinal anesthesia

NCT ID: NCT03719456 Completed - Renal Stone Clinical Trials

Prospective Assessment of Procedure-Related and Patient-Reported Outcomes After Retrograde Intrarenal Surgery (RIRS) for Renal Calculi Less Than 20 mm

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

The investigators aim at this study to prospectively assess procedure-related outcomes after RIRS for renal calculi less than 20 mm, including stone free rate (SFR), predictors of successful outcome, complications types/rate, readmission rate and the need of auxiliary procedures. In addition, patient-reported outcomes after this modality of intervention are going to be assessed.

NCT ID: NCT03373617 Completed - Renal Stone Clinical Trials

The Effect of Anesthesia Type on RIRS

Start date: December 13, 2017
Phase:
Study type: Observational [Patient Registry]

Retrograde intrarenal surgery (RIRS) with flexible ureteroscopy is based on video monitoring of urinary tract during operation. Therefore, shaking vision on monitor can bother surgeons and make them tired. This can lead in tissue injury from lasing. The purpose of this study is to investigate the stability of monitoring of surgical field which is assessed by surgeon.

NCT ID: NCT03349099 Completed - Urolithiasis Clinical Trials

Impact Ureteral Sheath Design During Ureteroscopy

Start date: June 27, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether one of two ureteral access sheaths is safer for patients undergoing ureteroscopy. Both sheaths are FDA approved devices and commercially available. The investigators will compare the ability of sheaths to access the kidney through the ureter and will compare damage done to the ureter after completion of the procedure. Access sheaths are standard of care for this procedure; this study seeks to optimize outcomes for patients. Patients undergoing ureteroscopy who do not have ureteral stents in place and who have not had an ipsilateral procedure within 90 days will be recruited and consented.

NCT ID: NCT03318926 Completed - Renal Stone Clinical Trials

Increased Tea Consumption is Associated With a Decreased Risk of Renal Stone Disease in a Taiwanese Population

Start date: June 2001
Phase: N/A
Study type: Observational

The objective of the this study was to examine the amount and duration of tea consumption in relation to the risk of renal stone disease.