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Kidney Calculi clinical trials

View clinical trials related to Kidney Calculi.

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NCT ID: NCT04122196 Active, not recruiting - Pain, Postoperative Clinical Trials

Perioperative Pregabalin in Ureteroscopy

Start date: June 1, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

This is a randomized, placebo-controlled, double-blinded study examining the use of perioperative pregabalin in ureteroscopy with stent placement. Ureteroscopy is typically performed for kidney or ureteral stones, but may be performed for other reasons such as for the diagnosis and possible treatment of certain kinds of cancers. As part of the same surgery, a ureteral stent is often placed. The surgery and the stent can cause discomfort, and patients may receive narcotic pain medicine. In other surgeries, a single dose of pregabalin, around one hour before surgery has been shown to decrease the need for pain medication after the surgery. This work will test whether this is true in ureteroscopy by giving eligible patients who agree to participate either pregabalin or a placebo shortly before surgery then examining how much pain medication they use after surgery. A placebo is an inactive medication. Neither the study participant nor the study staff will know who received pregabalin and who received placebo until after the study is over. For completing surveys, patients will receive compensation for their time in the form of gift certificates.

NCT ID: NCT04095975 Completed - Kidney Stone Clinical Trials

Effectiveness of Urinary Alkalinizing Agents on Kidney Stone Risk

Start date: August 28, 2019
Phase: Phase 4
Study type: Interventional

Randomized treatment trial of baking soda or LithoLyte to determine if baking soda and Litholyte are effective in raising 24 hour urine citrate and pH.

NCT ID: NCT04080973 Not yet recruiting - Osteopenia Clinical Trials

Metabolic Workup in Patients Suffering From Kidney Stone Disease and Osteopenia

Start date: October 2019
Phase: N/A
Study type: Interventional

Patients suffering from acute renal colic are evaluated by non contrast computerized tomography with excellent identification rates of urinary stones. The scan also covers the bones of the ribs, spine and pelvis, allowing measurements of the bone density and identifying early osteopenic changes. Bone demineralization is associated with metabolic changes such as hypercalcemia or hypercalcuria. In this study the investigators will look for correlation between kidney stones, osteopenic bone changes and metabolic abnormalities.

NCT ID: NCT04073719 Not yet recruiting - Clinical trials for Kidney Stones, Urolithiasis, Hypocitraturia

Apple Cider Vinegar for the Prevention of Urinary Lithiasis (APUL)

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

The purpose of this study is to assess whether certain beverages can increase urinary citrate levels in healthy individuals with no history of kidney disease.

NCT ID: NCT04071340 Enrolling by invitation - Renal Stone Clinical Trials

The Natural History of Minimally Symptomatic Nonobstructing Calyceal Stones

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

- The primary aim is to study the natural history of single-calyx asymptomatic nonobstructing stone disease. - The Secondary aim is to determine the predictors of the need for intervention and of cure in such population.

NCT ID: NCT04069338 Completed - Urolithiasis Clinical Trials

Comparison of Lithotripsy Urolithiasis Machines

CoLUM
Start date: May 31, 2019
Phase: N/A
Study type: Interventional

A comparison on the outcomes of patients undergoing shockwave lithotripsy using the Storz machine versus the Dornier machine.

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: NCT04051346 Active, not recruiting - Kidney Stone Clinical Trials

Dietary Oxalate and Innate Immunity in Kidney Stone Disease

Start date: March 5, 2021
Phase: N/A
Study type: Interventional

This study will test whether oxalate stimulates urinary crystals and impacts the immune system in healthy subjects using two controlled diets (low and high oxalate).

NCT ID: NCT03999255 Completed - Kidney Stone Clinical Trials

SEARCH FOR OPTIMAL ANAESTHESIA IN RETROGRADE INTRARENAL SURGERY

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

Patients undergoing retrograde intrarenal surgery for kidney stones from November 2017 to May 2018 were prospectively recruited to participate in the study. In each case after the beginning of general anesthesia with mechanical ventilation surgeons were asked to assess the mobility of the operative field and conditions for laser lithotripsy according to the developed questionnaire scale. The questionnaire consisted of 5 degrees of assessment of kidney mobility and each question was scored from 1 to 5, 1 being very mobile (extremely poor conditions for dusting) and 5 completely immobile (Ideal conditions for dusting). After this assessment modified technique of general anesthesia was applied called combined respiratory support which consisted of reduction of tidal volume to 250-300 ml and respiratory rate to 4-5 per minute with transcatheter high frequency jet ventilation through endotracheal tube with a respiratory cycle frequency of 300 per minute and maintained during retrograde intrarenal surgery. At the beginning of combined respiratory approach, surgeons were once again asked to assess the mobility of the operative field and the conditions for laser lithotripsy. Main ventilation parameters were recorded and compared in both regimens.

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.