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Calculi clinical trials

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NCT ID: NCT00762424 Completed - Kidney Stone Clinical Trials

Effect of Tamsulosin on Stone Expulsion and Pain Resolution in ED Patients With Ureterolithiasis

Flowmax
Start date: June 2007
Phase: N/A
Study type: Interventional

Tamsulosin (Flowmax)is approved by the FDA for the treatment for enlarged prostate. Several studies regarding the use of Tamsulosin for the treatment of lower kidney stones have been carried out in the non-Emergency Department setting. This study will compare Tamsulosin 0.4 mg with placebo in regards to rate and time of stone passing and will also look at amount of pain. The purpose of this study is to compare the usefulness of Tamsulosin versus placebo on time to stone passage and pain relief in Emergency Department patients with kidney stones.

NCT ID: NCT00639574 Completed - Clinical trials for Ureteral Calculi, Hyperalgic, Not Complicated

Nefopam and Morphine Consumption in the Treatment of Ureteral Calculi

Start date: March 2008
Phase: Phase 4
Study type: Interventional

The administration of néfopam after initial treatment by kétoproféne, could obtain, in patients remaining pain and classically need morphine, analgesia at least the same as morphine alone. The use of néfopam second line after ketoprofen could reducing (or even eliminating) the need for morphine (and its side effects), allowing a reduction in the length of stay of patients in the emergency unit. The main objective is to show that the addition of a néfopam initial treatment with the kétoproféne, reduces, in patients with ureteral calculi, the percentage of patients requiring the use of a treatment by morphine. The secondary objective is to reduce the side effects caused by the morphine, shorten the time to install the appropriate level of analgesia while reducing the risk of failure of the titration morphine, reduce the time spent on titration of morphine and reduce the length of stay patient intake in emergency unit.

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: NCT00599664 Completed - Urinary Calculi Clinical Trials

Pharmacokinetic and Safety Study of OMS201 in Subjects Undergoing Ureteroscopic Treatment for Removal of Urinary Tract-Located Stones

Start date: December 2007
Phase: Phase 1
Study type: Interventional

Evaluate the safety and systemic absorption of OMS201 following exposure during ureteroscopy.

NCT ID: NCT00495989 Completed - Disabled Persons Clinical Trials

Saliva and Dental Calculus in Handicapped People

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

This is an evaluation of potential differences in saliva composition and dental calculus composition between orally fed and tube fed individuals in an institutional environment.

NCT ID: NCT00448123 Completed - Kidney Stones Clinical Trials

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

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

To determine if emergency department patients with acute ureteral colic pain due to a ureteral stone who are treated with tamsulosin, versus placebo, will experience a shorter time to passage of their stone or resolution of their pain. A secondary study objective will be to determine if there is a relationship between response to tamsulosin and stone size or position in the ureter.

NCT ID: NCT00360477 Completed - Kidney Calculi Clinical Trials

FloSeal Tubeless Exit Versus Cope Loop Nephrostomy Versus Fascial Stitch Following Percutaneous Nephrolithotripsy

Start date: June 2004
Phase: N/A
Study type: Interventional

The patient will be asked to participate in a research project designed to determine the best way to prevent bleeding and promote patient comfort after having kidney stones removed. Two standard methods for ending the surgery are being compared to a newer method. In one standard method, the patient will have a tube draining urine from the kidney after the procedure. This tube may also prevent bleeding from the kidney. In another standard method the patient will have a tube left internally that drains urine from the kidney to the bladder and a stitch will be used to close the incision and deeper tissues in the back. In the third potential option, a tube would be left internally to drain urine from the kidney to the patient's bladder and the surgical site would be filled with a clot promoting agent (FloSeal) which is a FDA approved agent specifically formulated to stop bleeding during surgical procedures.

NCT ID: NCT00310908 Completed - Renal Calculus Clinical Trials

Comparison Between Tramadol Hcl and Other Analgesics in the Treatment of Renal Colic

Start date: September 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether Tramadol Hcl is as effective as Voltaren a non-steroidal antiinflammatory drug, and Dipyrone in amelioration of the pain caused by acute renal colic.

NCT ID: NCT00199459 Completed - Urinary Calculi Clinical Trials

Proteomic Study of Urinary Stone Disease

Start date: January 2005
Phase: N/A
Study type: Observational

Urinary protein levels are not routinely measured in stone patients while there is strong evidence that proteins play a role in the etiology of stones. The purpose of this study is to examine the urinary and serum proteins of stone formers compared to healthy subjects utilizing the high throughput method, Surface Enhanced Laser Desorption/Ionization (SELDI). We hypothesize that there is a unique set of proteins expressed in serum and urine in stone patients that can be detected by SELDI. Ultimately, this will better our understanding of stone disease and help develop new prevention strategies.

NCT ID: NCT00177086 Completed - Kidney Calculi Clinical Trials

Alfuzosin Hydrochloride to Promote Passage of Distal Ureteral Calculi

Start date: September 2005
Phase: Phase 3
Study type: Interventional

This study will assess improvement in the percentage of spontaneous stone passage for distal ureteral calculi for alfuzosin compared to placebo, decrease of pain and narcotic/analgesic use associated with stone passage, decrease of the time to spontaneous stone passage, shift in the size distribution of stones passed towards larger sizes.