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Urinary Calculi clinical trials

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NCT ID: NCT04610840 Recruiting - Urolithiasis Clinical Trials

The Use of Direct Puncture Technique With Mini-PCNL

Start date: July 1, 2020
Phase: N/A
Study type: Interventional

- A single-center randomized study to evaluate the safety and effectiveness of direct puncture of the caliceal system in mini-percutaneous nephrolithotripsy. - 60 patients - Inclusion criteria: 1. all patients aged 18 to 70 years who are planning mini-PCNL, ready to consent to the study 2. ASA scale 1-3 3. Solitary stone up to 2.5 cm 4. Single access to the caliceal system - Exclusion criteria: 1. Active infectious process 2. Coagulopathies 3. Abnormalities of the urinary system

NCT ID: NCT04598971 Recruiting - Clinical trials for Urinary Tract Infections

Urine pH and Urinary Tract Infection

PHURINE
Start date: August 1, 2020
Phase:
Study type: Observational

Urinary tract infections (UTI) affect the urine pH and may lead to salt precipitation such as struvite. Bacteria with urease activity are known to alkalinise urine, but not much is known on how pH is changing over time during UTI. This study aims at following urine pH progression at the time of diagnosis of UTI and during the treatment phase. Description of the change in urine pH over time will help understanding the risk of struvite formation and potential timing of intervention.

NCT ID: NCT04570787 Recruiting - Urolithiasis Clinical Trials

Bladder Catheterization After Mini-PCNL

Start date: July 1, 2020
Phase: N/A
Study type: Interventional

60 patients Inclusion Criteria: - age from 18 to 70 years - Indications for mini-PCNL - ASA score: 1-3 - Single percutaneous access to pyelocaliceal system - Size of solitary calculus up to 2.5 cm Exclusion Criteria: - Active urinary tract infection - Coagulopathy - Clinically significant infravesical obstruction (Qmax less than 10 ml / s, PVR more than 50 ml)

NCT ID: NCT04506723 Recruiting - Urolithiasis Clinical Trials

Comparison of Morphological and Radiological Data in Patients With Urolithiasis

Start date: April 30, 2020
Phase: N/A
Study type: Interventional

The aim of the study was to compare the ultrastructural changes in the renal parenchyma with the results of postprocessing CT analysis with contrast enhancement in patients with urolithiasis.

NCT ID: NCT04158570 Recruiting - Clinical trials for Upper Urinary Tract Stones

Role of Nephrolithometric Scoring Systems in Prediction of PCNL Outcomes in Adult

Start date: October 25, 2019
Phase:
Study type: Observational

Prospective study is to compare between different nephrolithometric scoring systems in prediction of PCNL outcomes in terms of efficacy , success rate and safety in Adult patients with UUT stones unilateral or bilateral, single or multiple, Pelvic or calyceal, primary or recurrent, both gender attending Assuit Urology & Nephrology University Hospital.

NCT ID: NCT04021381 Recruiting - Urolithiasis Clinical Trials

Citrate Salts for Stone-free Result After Flexible Ureterorenoscopy for Inferior Calyx Calculi

CiRUS
Start date: September 25, 2020
Phase: Phase 3
Study type: Interventional

The prevalence of urolithiasis is around 10 % in the French population. It is thus a major public health issue. When the stone is not spontaneously removed, interventions such as extracorporeal lithotripsy or flexible ureteroscopy (F-URS) are performed. F-URS is usually preferred in renal stones > 7 mm in comparison with lithotripsy, with better results. Efficacy of ureteroscopy is based on the "stone-free rate" (SFR) at 3 months. A SFR index is assessed according to the existence of residual fragments and their size. SFR score 1 (fragment ≤ 1mm) has been poorly studied, and is supposed to occur in 60% of cases. These residual fragments account for the high frequency of recurrence, probably favored by crystals aggregation and growth of these fragments under supersaturated urines. Indeed, calcium stones risk factors are urine supersaturation and crystal growth inhibitors deficiency. Citrate is the major crystal growth inhibitor in human urine. A hypocitraturia is reported in half of the lithiasic population. Consequently, citrate salts appear as an interesting therapeutic option, in order to slow crystal growth but also to chelate calcium, and consequently to solubilize stones in situ. However, to date, there is no available controlled study after surgical intervention such as flexible ureteroscopy. The aim of the investigator's study is to evaluate the efficacy of a 3-month potassium and magnesium citrate treatment following ureteroscopy on the elimination of residual fragments (SFR score 1).

NCT ID: NCT03846011 Recruiting - Urolithiasis Clinical Trials

Comparison of 24-hour Collecting Urine Prior and After Stone Removal

Start date: March 1, 2019
Phase:
Study type: Observational

The metabolic evaluation is crucial for determining possible underlying diseases causing stone growth and to consider the lifestyle changes or medical prophylaxis needed to prevent or at least reduce stone recurrence. 24-hour urine collection is the main part of the metabolic evaluation. The time point is suggested between 3 weeks and 3 month after stone removal, but so far there are no studies comparing 24-hour urine prior and after stone removal. In this study, investigators would like to analyze parameters in the 24-hour urine prior and after complete stone removal to see whether metabolic status can be evaluated no matter stone free or not.

NCT ID: NCT03257306 Recruiting - Kidney Stone Clinical Trials

Magnetic Ureteral Stent Symptoms - a Comparison to Standard Ureteral Stent as Perceived By the Patient (MAGUSS)

MAGUSS
Start date: November 9, 2018
Phase: N/A
Study type: Interventional

The specific aim of this study is to validate our hypothesis that the magnetic ureteral stents have the same amount of adverse effects as the more commonly used non-magnetic ureteral stents. If this hypothesis would be confirmed then the usage of magnetic ureteral stents would be justified for both reducing patient discomfort by way of fewer cystoscopies and possibly also decreasing the overall expenditures of treatment.

NCT ID: NCT03108053 Recruiting - Urinary Stone Clinical Trials

Results of Safety Guidewire Use in Ureteroscopic Stone Surgery

Start date: June 1, 2014
Phase: N/A
Study type: Interventional

Up-to-date, urology guidelines introduce safety guidewire (SGW) as an integral tool in ureteroscopy and recommended its routine use. However, the necessity of SGW placement in endourological procedures lack evidence and is being suggested as an expert opinion. Present study aimed to evaluate the use of SGW placement and its necessity in treatment of ureteral stones with semi-rigid ureteroscopy (s-URS). For this purpose patients with ureteral stones are being stratified according to ureteral stone location and prospectively randomized into two groups' according to SGW usage or not in s-URS. Ureteroscopy and litotripsy is being done with a semi-rigid ureteroscope of 6.4/7.8 Fr (Olympus) and laser. Chi-square and student t-test were used for comparing data.

NCT ID: NCT02594631 Recruiting - Urinary Calculi Clinical Trials

Shock Wave Lithotripsy Versus Visual Cystolitholapaxy in The Management of Patients Presenting With Calcular Acute Urinary Retention: A Randomized Controlled Trial.

Start date: March 2015
Phase: Phase 4
Study type: Interventional

The aim of the study is to compare the safety and efficacy of ESWL and visual cystolitholapaxy in management of calcular acute urine retention.