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Kidney Calculi clinical trials

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NCT ID: NCT04234035 Recruiting - Emergencies Clinical Trials

Shared Decision-Making for the Promotion of Patient-Centered Imaging in the ED: Suspected Kidney Stones

ED-KSS
Start date: December 11, 2019
Phase: N/A
Study type: Interventional

Although a CT scan is required for some Emergency Department patients with signs and symptoms of a kidney stone, recent evidence has shown that routine scanning is unnecessary and may expose young patients to significant cumulative radiation, increasing their risk of future cancers. Shared Decision-Making may facilitate diagnostic imaging decisions that are more inline with patients' values and preferences. By comparing a shared approach to diagnostic decision-making to a traditional, physician-directed approach, this study lays the foundation for a future randomized trial that will reduce radiation exposure, improve engagement, and improve the quality and patient-centeredness of Emergency Department care.

NCT ID: NCT04069013 Recruiting - Kidney Diseases Clinical Trials

Standard vs Mini-PCNL for the Treatment of Stone Disease

Start date: May 1, 2022
Phase: N/A
Study type: Interventional

Randomized comparison of patient outcomes following standard PCNL versus mini-PCNL.

NCT ID: NCT03995758 Recruiting - Kidney Calculi Clinical Trials

MOSES Lithotripsy Technology Applied to Stone Fragmentation During Ureteroscopy

Start date: June 6, 2019
Phase: N/A
Study type: Interventional

To determine if the effects of MOSES laser modulation technology can improve the safety and efficiency to laser fragmentation resulting in decreased total laser time, reduced potential for injury to the patient, and total OR time and utilization.

NCT ID: NCT03951558 Recruiting - Nephrolithiasis Clinical Trials

Comparison of the Impact of Diet vs Thiazide in BMD in Children With Idiopathic Hypercalciuria

HIC
Start date: May 11, 2018
Phase: N/A
Study type: Interventional

The investigator's objective is to compare and evaluate the impact of nutritional treatment vs. pharmacological treatment (hydrochlorothiazide) in bone mineral density in children with idiopathic hypercalciuria. A randomized, open-label, one-year follow-up study will be conducted in children aged 5 to 21 years with a confirmed diagnosis of idiopathic hypercalciuria or lithiasis, excluding those patients with secondary hypercalciuria (primary hyperoxaluria, treatment with vitamin D, Bartter syndrome, primary hyperparathyroidism), previous kidney transplantation. The impact of diet (hyposodic, calcium intake according to DIR for age, normal protein intake and high water intake) will be evaluated vs. the pharmacological treatment (hydrochlorothiazide) on bone mineral density.

NCT ID: NCT03924362 Recruiting - Clinical trials for Nephrolithiasis of Both Kidneys

Bilateral Percutaneous Nephrolithomy

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

The purpose of this study is to determine the effective regimen for definitive surgical therapy of bilateral kidney stones. It is unknown whether patients who undergo simultaneous bilateral percutaneous nephrolithotomy (PCNL) experience improved post-operative outcomes compared to patients who have staged unilateral procedures.

NCT ID: NCT03855787 Recruiting - Kidney Calculi Clinical Trials

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

Start date: November 11, 2019
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT03797027 Recruiting - Kidney Stone Clinical Trials

Effects of Abdominal Cushion on PCNL in Prone Position

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

Percutaneous nephrolithotomy (PCNL) is the first choice for the treatment of ≥ 2cm renal stones. The positions of PCNL includes supine, prone and lateral. PCNL has been performed in my center for nearly twenty years. The prone position is routinely used. Generally speaking, an abdominal cushion is used to raise the abdominal in the prone position, in order to provide an adequate exposure of kidney, increase the intercostal space, decrease the mobility of kidney and lower the risk of pleura injury. However, there is no consensus and criterion on the height of abdominal cushion. With largely increased PCNL procedures and various BMI, precise evaluation of abdominal cushion is needed. In the preliminary work, the investigators measured the sunken height of waist of 100 patients in the prone position without a abdominal cushion. The results showed that the mean BMI of 100 patients was 23.45 (16.79-36.98) and the range of sunken height of waist was 2-7 cm. Therefore, the investigators are planning to conduct a randomized controlled study to compare the safety and efficacy among no cushion group, 5 cm cushion group and 10 cm cushion group. To clarify the relationship between height of abdominal cushion and BMI, the nurse could prepare the appropriate cushion the day before surgery, which would decrease operating time and accelerate postoperative recovery.

NCT ID: NCT03795532 Recruiting - Renal Stones Clinical Trials

Ultraslow SWL Versus Slow SWL for Renal Stones With High Attenuation Value

ESWL
Start date: January 11, 2019
Phase: N/A
Study type: Interventional

Ultraslow full-power SWL versus slow power-ramping SWL in Renal stones with high attenuation value

NCT ID: NCT03704350 Recruiting - Kidney Stone Clinical Trials

Influence of Obesity on Endogenous Oxalate Synthesis

Start date: May 24, 2019
Phase: N/A
Study type: Interventional

There is increasing evidence that obesity is associated with increased urinary oxalate excretion, an important risk factor for calcium oxalate stone formation. By the administration of a controlled low oxalate diet the investigators will estimate endogenous oxalate synthesis in both non-obese and obese non-kidney-stone forming adults. This study seeks to thusly increase the understanding of the relationships between obesity and endogenous oxalate synthesis to serve as a platform to develop novel therapies for stone prevention.

NCT ID: NCT03692715 Recruiting - Nephrolithiasis Clinical Trials

Antibiotic Prophylaxis Before Shock Wave Lithotripsy

APPEAL
Start date: September 27, 2018
Phase: Phase 4
Study type: Interventional

This is a two arm, double blind RCT comparing the use of a single dose ciprofloxacin prior to SWL to saline alone. The multicenter trial will be conducted with a pragmatic emphasis including both high volume and low volume sites internationally.