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Water-electrolyte Imbalance clinical trials

View clinical trials related to Water-electrolyte Imbalance.

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NCT ID: NCT06013800 Recruiting - Hyponatremia Clinical Trials

Hyponatremia Volume Status Analysis by Point-of-care Ultrasound

Vostaus
Start date: October 1, 2023
Phase:
Study type: Observational

This observational study aims to analyze the time of correction of hyponatremia in patients within an internal medicine ward. The researchers will assess volume status using both clinical evaluation and point-of-care ultrasound. Patients will be categorized based on whether they have the same volume status determined clinically and by ultrasound or a different status between the two methods. By tracking sodium levels daily until normalization, the study will compare the time of hyponatremia correction between the two groups.

NCT ID: NCT05772364 Recruiting - Orthopedic Disorder Clinical Trials

High- Versus Low-calcium Water for Bone Health

Start date: March 2, 2023
Phase: N/A
Study type: Interventional

The experimental study investigates which metabolic responses of calcium and parathyroid hormone are observable in blood and urine in a cohort of 41 healthy adults following a sequence of different exposures: low-calcium water first and high-calcium water afterward.

NCT ID: NCT05129930 Completed - Critical Illness Clinical Trials

Fluid Overload and Pulmonary Function

Start date: December 1, 2020
Phase:
Study type: Observational

Esophageal atresia is a rare but severe malformation, and it requires early surgery. Coloesophagoplasty is surgical repair of the esophageal with an isoperistaltic transverse colon graft. In the postoperative period after coloesophagoplasty children require careful monitoring of fluid balance, because clinically significant fluid overload can lead to dysfunction of various organs and systems.

NCT ID: NCT04937465 Withdrawn - Clinical trials for Dehydrated, Water-Electrolyte Imbalance, Malnutrition

Explorative Study on a New Device' Ability to Register Hydration Change in Elderly Subjects During Rehabilitation.

Start date: November 1, 2021
Phase:
Study type: Observational

Test the ability of continuous measurements from a new sensor patch to set the hydration state in subjects who are malnourished/dehydrated or overhydrated or otherwise not optimally hydrated. Specifically, clinical examination, blood pressure, blood tests, and weight change at the admission and at the discharge will be used to establish the true hydration status of the subjects.

NCT ID: NCT04799067 Completed - Hemodialysis Clinical Trials

Hyperkalaemia Prevalence, Recurrence and Treatment in Haemodialysis

PRECEDE-K
Start date: May 17, 2021
Phase:
Study type: Observational

The objective of this study is to evaluate the prevalence and recurrence of Hyperkalaemia (HK) in Chinese HD patients and to understand the treatment pattern of HK in China.

NCT ID: NCT03142464 Completed - Clinical trials for Postoperative Nausea

Intravenous Fluids After Laparoscopic Cholecystectomy

Start date: July 1, 2015
Phase: N/A
Study type: Interventional

Perioperative intravenous fluid (IV) administration has been the standard procedure since 1832 and, is a widely used practice sometimes under inadequate criteria. The present work aims at verifying the clinical need that justifies the common IV fluid prescription on the postoperative (PO) period in patients undergoing videolaparoscopic cholecystectomy (CVL) elective.

NCT ID: NCT03141632 Completed - Thirst Clinical Trials

Effects of Glucagon Like Peptide 1 (GLP-1) Analogues on Fluid Intake

GATE
Start date: October 17, 2016
Phase: Phase 2
Study type: Interventional

The aim of this study is to elucidate whether GLP-1 analogues influence not only appetite but also thirst perception. It is hypothesized that GLP-1 analogues reduce fluid intake in healthy volunteers compared to Placebo.

NCT ID: NCT03080831 Completed - Fluid Overload Clinical Trials

TOnicity of Perioperative Maintenance SoluTions

TOPMAST-1
Start date: March 9, 2017
Phase: Phase 4
Study type: Interventional

Prospective randomized double blind phase IV trial studying the efficacy and safety of the tonicity of two different perioperative maintenance solutions: an isotonic solution containing NaCl 0.9 in glucose 5% with an added 40 mmol/L of potassium or a commercially available premixed solution (Glucion 5%) containing a.o. 54 mmol/L of sodium and 26 mmol/L of potassium. Both solutions are administered at 27 mL/kg of ideal body weight, as recommended by current guidelines (NICE 174) and both solutions are widely used in daily clinical practice. The primary hypothesis is that isotonic maintenance solutions lead to more fluid retention than hypotonic fluids. Metabolism of both solutions is assessed by sequential analysis of urine and serum and clinical parameters.

NCT ID: NCT01626040 Completed - Clinical trials for Water-Electrolyte Imbalance

Evaluation of One-day Polyethylene Glycol Powder Solution for Colonoscopy in Children

Start date: June 2012
Phase: N/A
Study type: Observational

The purpose of this study is to examine the effects of current standard of care Polyethylene Gylcol powder (PEG-P)colonoscopy preparation on a patient's serum electrolytes, tolerance of the prep, and how well the bowel is cleansed. The primary aim is to determine the proportion of patients with clinically significant serum electrolyte abnormalities at the time of colonoscopy and how well the prep is tolerated. Secondary objectives include: 1) how well the bowel is cleansed with this preparation, and 2) to determine the most effective way to communicate instructions about the bowel preparation with the child and family.

NCT ID: NCT01087853 Completed - Fluid Overload Clinical Trials

The Effect of Crystalloids and Colloids on Visceral Blood Flow

Start date: March 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Patients often require fluid replacement during and after an operation. This is usually given through veins in the arm using an intravenous cannula and doctors have traditionally used fluid containing sodium chloride (saline). However accumulating evidence suggests that large infusions of saline are associated with adverse physiological effects including acidification of the blood and a rise in potassium and chloride levels. Studies in animals have shown that high levels of chloride in the blood and excess saline can cause blood vessels in the kidney to constrict leading possibly to a decrease in kidney function. Improvement in acid-base balance and kidney function may be observed with balanced solutions containing constituents that are more closely matched to the body's own fluid composition. However, little is known about the physiological effects of these solutions as they have only recently been developed. Magnetic resonance imaging (MRI) is a radiological modality which can now assess blood flow and supply of the kidney noninvasively without the need for the injection of radiological dyes known as contrast agents. This is now of major importance due to the possible adverse effects of MRI contrast agents leading to Nephrogenic Systemic Fibrosis (NSF), a progressive disease which has been observed in some kidney patients after receiving 'gadolinium based' contrast agents. This has therefore led to increased interest and demand for noncontrast based imaging methods. In this study we aim to compare the effects of balanced versus unbalanced fluid infusions in healthy human volunteers: We will aim to measure: 1. Blood biochemical composition and acidity 2. Kidney function and supply as measured by dynamic MRI