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Kidney Calculi clinical trials

View clinical trials related to Kidney Calculi.

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NCT ID: NCT03130907 Completed - Ureteroscopy Clinical Trials

The Role of Ureteral Stenting Following Uncomplicated Ureteroscopy for Ureteral and Renal Stones: A Randomized, Controlled Trial

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

It is well established that uncomplicated distal ureteroscopy can be safely performed without leaving a ureteral stent. However, many urologists continue to leave ureteral stents following uncomplicated ureteroscopy, regardless of stone location, due to concerns for post-operative complications, patient symptoms and to reduce unplanned medical visits. There is a paucity of data regarding the utility of stent placement for proximal ureteral or renal stones following ureteroscopy. We have designed a prospective, randomized controlled trial to evaluate the role of ureteral stent placement following ureteroscopy and pyeloscopy in proximal and renal stones.

NCT ID: NCT03112499 Completed - Renal Insufficiency Clinical Trials

The Effect of Three Endourological Procedures for the Management of Renal Calculi Regarding Acute Kidney Injury

Start date: June 5, 2018
Phase: N/A
Study type: Interventional

The main aim of the study is to investigate and compare the possible acute effect of standard PCNL, mini-PCNL and RIRS on renal function. Secondary aims are to investigate the efficacy (stone-free rate), safety (complication rate, long-term kidney function) and other parameters (operation, fluoroscopy and hospitalization time) concerning the 3 endourological operations (PCNL, mini- PCNL, RIRS) for the treatment of renal calculi.

NCT ID: NCT03111381 Completed - Pain, Postoperative Clinical Trials

Toradol to Reduce Ureteroscopic Symptoms Trial

TRUST
Start date: August 1, 2017
Phase: Phase 2
Study type: Interventional

Double blinded randomized controlled clinical trial to assess the impact of intraoperative Toradol on post-operative pain scores for patients undergoing ureteroscopy for urinary stone management.

NCT ID: NCT03095885 Completed - Nephrolithiasis Clinical Trials

A Pilot Study of Oxalate Absorption in Secondary Hyperoxaluria

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

Identify individuals with greater absorption of oxalate based on increase in urinary oxalate excretion in response to a controlled oxalate-rich test meal.

NCT ID: NCT03087812 Completed - Kidney Stones Clinical Trials

Durability of Flexible Ureteroscopes and Causes of Infection During Flexible Ureterorenoscopy

Start date: December 2015
Phase:
Study type: Observational

This is an observational study in which data on consecutive patients who undergo ureterorenoscopy with the use of a flexible ureterorenoscope are collected. In total 20 new ureteroscopes are usedfrom Olympus andfrom Storz) to study the durability of the ureteroscopes and the possible microbiological load.

NCT ID: NCT03087149 Completed - Clinical trials for Vitamin D Deficiency

Monitored vs Standard Supplementation of Vitamin D in Preterm Infants

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

The purpose of this study is to determine wheather the monitored vitamin D (vit D) therapy is safer and more effective than standard therapy in pretrem infants.

NCT ID: NCT03057431 Completed - Nephrolithiasis Clinical Trials

Hydrochlorothiazide for Kidney Stone Recurrence Prevention

NOSTONE
Start date: March 9, 2017
Phase: Phase 3
Study type: Interventional

The investigators plan to assess the efficacy of standard and low dose HCTZ treatment in the recurrence prevention of calcium-containing kidney stones. More specifically, the investigators aim to assess the dose-response relationship for three different dosages of HCTZ. Study intervention: HCTZ 12.5 mg, 25 mg or 50 mg once daily per os for 24 or 36 months. In addition, all patients in HCTZ treatment arms will receive state-of-the-art non-pharmacologic recommendations for stone prevention according to current guidelines. Control intervention: Placebo once daily per os for 24 to 36 months. In addition, all patients in the placebo arm will receive state-of-the-art non-pharmacologic recommendations for stone prevention according to current guidelines.

NCT ID: NCT03046888 Completed - Renal Stone Clinical Trials

ROBOTIC PYELOLITHIOTOMY VERSUS PERCUTANEOUS NEPHROLITHOTOMY (PCNL).

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

Prospectively randomized study in patients with renal pelvic stones who are candidate to standard PCNL procedure. One to one, controlled clinical trial. Patients will be randomly allocated into two groups, 20 patients in each group. Group A will be scheduled to receive routine standard PCNL. Group B will be scheduled to receive Robot assisted pyelolethotomy.

NCT ID: NCT03040466 Completed - Kidney Calculi Clinical Trials

Comparing Treatment of Urolithiasis Between Disposable and Reusable Ureteroscope

Start date: August 2014
Phase: N/A
Study type: Interventional

Reusable flexible ureteroscopes are widely used to treat various upper urinary tract diseases including urinary stones. However, they require a long turnover time between procedures because of the sterilization process. Moreover, repeated use of a scope ultimately deteriorates its image quality which leads to a high maintenance cost in the long-term. A disposable digital flexible ureteroscope was released in the United States in January 2016, offering an improved image resolution, new scope performance characteristics with every case, and no need for sterilization and repair. Preliminary data from our center has demonstrated that disposable scopes shorten operative time by 25% compared to reusable fiberoptic scope and are associated with a 2/3 reduction in procedural complication rate. Therefore, treatment with disposable scopes may be more effective for patients and facilitate cost management within the hospital. Here, we propose a three-armed, prospective randomized study, comparing treatment outcomes between disposable digital, reusable fiberoptic, and reusable digital flexible ureteroscopes.

NCT ID: NCT03035812 Completed - Blood Pressure Clinical Trials

Alkalinization by Urologists & Nephrologists

AlcalUN
Start date: February 1, 2017
Phase: Phase 4
Study type: Interventional

Metabolic acidosis recovers a wide range of diseases in which an oral alkalinization could be useful. This therapeutic intervention has been said to increase extracellular volume leading to rising blood pressure. No prospective data has been published in clinical routine. Here, investigators propose to follow patients in which an oral alkalinization is indicated: blood pressure, body weight, and a clinical evaluation of the extracellular compartment will be performed at the beginning and during the follow-up of participants. The principal criterion of evaluation will be the variation in the extracellular compartment.