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Nephrolithiasis clinical trials

View clinical trials related to Nephrolithiasis.

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NCT ID: NCT00713739 Recruiting - Kidney Stones Clinical Trials

Alfuzosin for Medical Expulsion Therapy of Ureteral Stones

MET
Start date: January 2008
Phase: Phase 3
Study type: Interventional

The goal of this study is to conduct a prospective controlled trail of four currently approved Department of Defense (DOD) - formulary medications for use as medical expulsion therapy (MET) for kidney stones. Between 8% and 15% of Americans will develop symptomatic urolithiasis in there life. Several medications, including steroids, calcium channel blockers, alpha-adrenergic antagonists and non-steroidal anti-inflammatory drugs, have been utilized to aid in the spontaneous passage of distal ureteral calculi. Recently, use of selective alpha-blockers has shown promise for medical expulsion therapy (MET) of distal ureteral calculi. None of these studies have been widely publicized outside the specialty of urology. Recent studies have shown a success rate of nearly 90% when the selective alpha-blocker tamsulosin (Flomax) was used for MET. MET has also been shown to result in a decreased narcotic requirement, shorter time to stone passage, and reduced requirement for further interventions. The investigators will evaluate the effectiveness of MET as initial management for kidney stones using DOD-approved formulary medications.

NCT ID: NCT00638482 Terminated - Nephrolithiasis Clinical Trials

Dose-Dependent Effect of Thiazide in Dent's Disease Hypercalciuria

DESY
Start date: July 2003
Phase: Phase 2/Phase 3
Study type: Interventional

Intrarenal calcifications (nephrocalcinosis) is present in Dent's disease and likely contribute to progression toward renal failure. In order to prevent this complication it is usually proposed to treat affected patients during childhood with high doses of thiazides.

NCT ID: NCT00600405 Completed - Nephrolithiasis Clinical Trials

The Efficacy of Tamsulosin in the Treatment of Ureteral Stones in Emergency Department Patients

Start date: August 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of the α-adrenergic antagonist tamsulosin in the treatment of adult emergency department (ED) patients with ureteral colic secondary to lower ureteral calculus. We hypothesize that there will be no difference in outcomes for subjects treated with and without tamsulosin.

NCT ID: NCT00588562 Recruiting - Clinical trials for Primary Hyperoxaluria

Rare Kidney Stone Consortium Patient Registry

RKSC
Start date: July 2003
Phase:
Study type: Observational

The purpose of this study is to collect medical information from a large number of patients in many areas of the world with primary hyperoxaluria (PH), Dent disease, Cystinuria and APRT deficiency. This information will create a registry that will help us to compare similarities and differences in patients and their symptoms. The more patients we are able to enter into the registry, the more we will be able to understand the Primary Hyperoxalurias,Dent disease, cystinuria and APRT and learn better ways of caring for patients with these diseases.

NCT ID: NCT00587041 Completed - Crohn's Disease Clinical Trials

Use of Oral Probiotics to Reduce Urinary Oxalate Excretion

Start date: February 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study was to determine the effect of two probiotic preparations (Agri-King Synbiotic and Oxadrop) on urinary oxalate excretion in patients with mild hyperoxaluria. Probiotics are live microorganisms thought to be beneficial to the host organism. Hyperoxaluria is a hereditary disorder that causes a special kind of stone to form in the kidney and urine. Oxalates are naturally-occurring substances found in plants, animals, and in humans. Excretion of oxalates in the urine is a risk factor for kidney stone formation. Our hypothesis was that the mild hyperoxaluria is due to over absorption of oxalate from food and that probiotics will improve gastrointestinal barrier function to decrease oxalate absorption across the gut (and hence its elimination in the urine). In the study, participants were randomized to placebo, Agri-King Synbiotic, or Oxadrop, and were treated for 6 weeks. Patients were maintained on a controlled diet to remove the confounding variable of differing oxalate intake and availability from food.

NCT ID: NCT00583258 Withdrawn - Kidney Stones Clinical Trials

A Randomized Study of Whether Alfuzosin(Xatral) Helps in the Passage of Kidney Stones

Start date: October 2007
Phase: N/A
Study type: Interventional

Patients who present for the first time to Emergency Room with renal colic due to a distal ureteral calculus (as diagnosed with spiral CT scan and KUB) will be randomized to receive Xatral 10mg po once a day or placebo once discharged from the ER. The purpose of this study is to assess if patients treated with Xatral will have a higher spontaneous passage rate of their ureteral stone than those treated with placebo.

NCT ID: NCT00581178 Terminated - Kidney Stones Clinical Trials

Study to Determine if There Are Specific Clinical Factors to Determine Stent Encrustation

Start date: April 2008
Phase: N/A
Study type: Observational

Ureteral stent placement is one of the most common procedures performed within urology. The stents are generally placed for relief of obstruction or to prevent obstruction following a urological procedure. Most patients with ureteral stents will eventually form stent encrustations. However, patients form these encrustations at dramatically different degrees and rates ranging from no encrustation at 1 year of stenting to severe encrustation in just a few weeks. The purpose of this study is to determine if the degree of encrustation on a stent for any given patient can be predicted based on 24 hour urine parameters prior to stent placement, with the stent in place and after stent removal. Patients who will be receiving stents for other urological reasons will have a 24 hour urine sample collected before stent placement, while the stent is in place and after the stent has been removed. The parameters examined in the 24 hour urine collected will then be compared to the amount of encrustation there is on the stent to see if there is any correlation between the two.

NCT ID: NCT00504283 Completed - Kidney Stone Clinical Trials

An Analgesia Protocol for Acute Renal Colic in the Emergency Department

Start date: February 2007
Phase: N/A
Study type: Interventional

An analgesia protocol for acute renal colic will lead to faster significant reductions in pain than prior practice.

NCT ID: NCT00490113 Withdrawn - Kidney Stones Clinical Trials

A Trial of Pyridoxamine to Lower Urine Oxalate in Subjects With Stone Disease or Hyperoxaluria

Start date: January 2007
Phase: Phase 2
Study type: Interventional

To determine whether pyridoxamine can decrease oxalate excretion in subjects who have normal oxalate excretion (but who have had kidney stones), and in subjects who have primary hyperoxaluria.

NCT ID: NCT00489723 Recruiting - Kidney Stones Clinical Trials

Is There is a Role of Prophylactic Therapy With Tamsulosin Before Extracorporeal Shock Wave Lithotripsy to Avoid Development of Steinstrasse ?

Start date: May 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine if there is a role of prophylactic therapy with tamsulosin prior extracorporeal shock wave lithotripsy to avoid development of steinstrasse. 150 persons that will go to Extracorporeal shock wave lithotripsy will randomize to 2 groups. Group 1 -of 75 persons will recieve tamsulosin 0.4 mg x 1/d 2 days before the lithotripsy . Group 2 - of 75 persons will not recieve tamsulosin. 48 hour after the ESWL all 2 group will take abdominal radiograph to evaluate the presence of steinstrasse.