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Nephrolithiasis, Calcium Oxalate clinical trials

View clinical trials related to Nephrolithiasis, Calcium Oxalate.

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NCT ID: NCT02096965 Completed - Clinical trials for Nephrolithiasis, Calcium Oxalate

Use of Tolvaptan to Reduce Urinary Supersaturation: a Pilot Proof of Principle Study

Start date: March 2014
Phase: Phase 1
Study type: Interventional

In this study the investigators propose to use a daily dose of 45 mg (30 mg at 8 AM and 15 mg at 4 PM). This relatively small well-tolerated dose is likely to persistently increase urine volume and reduce urine supersaturation and to be well tolerated by patients with kidney stone disease and normal renal function (see below). The twice-daily (8 AM and 4 PM) regimen is designed to produce a maximal AVP inhibition on waking with a gradual fall-off of effect during the night. To this end, a higher dose is used in the morning, with a lower dose in the afternoon.

NCT ID: NCT00381849 Completed - Cystinuria Clinical Trials

Use of an Herbal Preparation to Prevent and Dissolve Kidney Stones

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

We will investigate the safety and effectiveness of a mixture of 9 east Indian herbs known as Cystone regarding their ability to dissolve existing kidney stones and prevent formation of new ones. Cystine and calcium stone formers will be recruited for a 59 week trial. The first phase of the study will be two 6 weeks periods during which each subject will receive Cystone or placebo in random order (with a one-week wash out between 6 week treatment periods). The remaining 46 weeks, each subject will receive Cystone. End points are changes in urinary chemistries and stone burden by Computerized Tomography (CT) scanning.