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Hypokalemia clinical trials

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NCT ID: NCT01269099 Completed - General Anesthesia Clinical Trials

Hypokalemia and Intravenous Patient Controlled Analgesia

Start date: January 2010
Phase: N/A
Study type: Interventional

The increase in stress hormone level and hyperventilation caused by the postoperative pain may contribute to the development of hypokalemia during postoperative period. Therefore, if the postoperative pain is well controlled by the IV-PCA,the plasma potassium level during the postoperative period may be not affected by stress response. The researchers tried to investigate the effect of IV-PCA on potassium regulation during the postoperative period.

NCT ID: NCT00718068 Completed - Clinical trials for Arrhythmias, Cardiac

Safety of Continuous Potassium Chloride Infusion in Critical Care

ASPIC
Start date: October 2008
Phase: Phase 4
Study type: Interventional

Patients in critical care often require supplemental potassium chloride if levels in their blood are below acceptable level. Common practice is to administer a single dose of potassium chloride under controlled conditions via a drip, before checking if a further dose is required. The purpose of this study is to ensure that it is safe to administer potassium chloride continuously with the dose varied according to patient needs.

NCT ID: NCT00605202 Completed - Hypokalemia Clinical Trials

Effect of Licorice and Hydrochlorothiazide on Plasma Potassium

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

This clinical trial is designed to study the effect of the combination of licorice and hydrochlorothiazide on plasma potassium levels in volunteers. In one arm, 10 healthy volunteers will be given 32 grams of licorice a day together with a 25 mg dose of daily hydrochlorothiazide for 14 days. This combination is compared with 32 grams of licorice a day for 14 days given in the other arm. The study is a randomized, open-label cross-over trial. There is at least a 3-week wash-out between the arms. The hypothesis is that the combination of licorice and hydrochlorothiazide will cause hypokalemia. The main outcome measure is the change in the plasma level of potassium between the arms.

NCT ID: NCT00276289 Completed - Clinical trials for Idiopathic Hypercalciuria

Spironolactone to Decrease Potassium Wasting in Hypercalciurics on Thiazides Diuretics

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

Kidney stone formation due to an excess of calcium in the urine is a common problem. It is treated with thiazide diuretics. These drugs often cause excessively low blood potassium levels that in turn require large doses of potassium supplements. These supplements are often large, unpleasant and easy to forget. We are trying the addition of spironolactone to these patients' medications to see if it allows them to take a lower dose of potassium.