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Dehydration clinical trials

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NCT ID: NCT04536324 Completed - Aged Clinical Trials

The Absorption Rate of Subcutaneous Infused Fluid

ABSU
Start date: September 1, 2020
Phase:
Study type: Observational

The purpose of the study is to examine the rate of absorption of subcutaneous infused fluid in older adults when acutely ill compared to when they are not acutely ill.

NCT ID: NCT04502238 Active, not recruiting - Clinical trials for Dehydration (Physiology)

Dehydration and Population Health

Start date: March 3, 2020
Phase:
Study type: Observational

The primary aim of this study is to assess cardiovascular changes (blood pressure, heart rate, electrocardiogram/ECG) in response to mild fluid-restriction dehydration and subsequent rehydration in healthy young and old people. Secondary aims are to assess changes in body composition, mood, and hunger in response to mild dehydration and rehydration.

NCT ID: NCT04372498 Completed - Clinical trials for Dehydrated Hereditary Stomatocytosis

Senicapoc and Dehydrated Stomatocytosis

Start date: April 15, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

Dehydrated stomatocytosis is a genetic disorder characterized by chronic hemolysis, variable anemia and erythrocyte dehydration. Causative mutations have been identified in either the Gardos (KCNN4) channel or the mechanosensitive channel PIEZO1. Senicapoc is a selective blocker of the Gardos channel that has been extensively studied in sickle cell disease and shown to be safe with limited side-effects. However, senicapoc did not meet the designated clinical endpoints in a pivotal phase 3 trial. The present study is an explanatory, proof-of-concept study of Senicapoc administered once daily in patients with familial dehydrated stomatocytosis caused by autosomal dominant V282 mutations in the Gardos (KCNN4) channel.

NCT ID: NCT04318847 Not yet recruiting - Clinical trials for Vomiting in Infants and/or Children

Efficacy and Safety of the Administration of Ondansetron Versus Habitual Clinical Practice for the Treatment of Vomiting in Children With Mild and Moderate Dehydration: Randomized Clinical Trial

Start date: October 10, 2021
Phase: Phase 4
Study type: Interventional

This clinical trial is intended to evaluate the efficacy and safety of the administration of ondansetron in children with mild-moderate dehydration. The target population will be children between 4 and 13 years old who present vomiting.

NCT ID: NCT04290598 Completed - Clinical trials for Color; Change Teeth, Posteruptive

Clinical Effects of Dehydration on Tooth Colour

Start date: October 14, 2019
Phase:
Study type: Observational

Dental restorations should mimic sound tooth structures in terms of color and optical properties especially in the anterior region. However, closely matching natural teeth with a restoration can be one of the most challenging procedure in restorative dentistry. Shade matching includes color determination, color communication with dental lab and color reproduction with dental restoration for indirect techniques or color determination and selection of the appropriate material and application method when using direct techniques. Therefore color selection is the first critical step in the restoration procedures and should be carried out properly. Color determination must be carried out before any of the restorative procedures, isolation or impression. Most of the dental procedures cause dehydration and increase the opacity of the enamel and teeth appear whiter. Few clinical and in vitro studies evaluated the degree of color change after dehydration and rehydration periods. However, inconsistencies exist between studies in terms of color change degree and duration of return to appreciable values. The aim of the present study was to evaluate the degree of color change in half an hour dehydration period of the teeth and to determine if color return to baseline after half an hour or 24 hours. According to the null hypotheses of the study: - There is no perceptible difference occur after tooth dehydration. - Tooth color will not return to baseline values after half an hour or 24 hours rehydration periods.

NCT ID: NCT04265300 Completed - Clinical trials for Dehydration in Children

Hydration Intervention in Children

Start date: January 6, 2020
Phase: N/A
Study type: Interventional

The investigators are conducting this research study to determine learn how daily habits and fluid choices impact children's health, sleep, cognitive function and mood. The investigators look to determine if a hydration intervention using an alternative beverage may impact these variables in children. Maintaining an appropriate level of hydration throughout the day has multiple health benefits. Maintaining a desirable hydration status improves overall health and wellbeing (mood, reaction time, sleep quality, cognitive function, etc.) in adults, but negative health and mental effects of hypohydration are not fully understood in an adolescent population. Maintaining appropriate hydration in adolescents presents unique challenges with respect to schedule (e.g. the availability of fluid during the school day and after school activities) as well as ensuring the most beneficial beverage choice. Adolescents can be very meticulous regarding their preferred beverage (e.g. choosing a sugary drink over water) and parents prefer their children consume the healthiest option for their food and beverages, often times leading to conflict. Therefore the purpose/goal of the proposed study is to determine if a hydration intervention using an alternative sweetened beverage will improve hydration and other overall health (e.g. cognitive function, sleep quality, mood etc.) The investigators hypothesize, that by giving children an alternative tasty option, they will consume more fluids which may lead to improving and maintaining their chronic hydration state. Implementing a beverage intervention with a sweet alternative option (i.e. Creative Roots) could improve hydration levels in adolescents. In turn, possibly improving mood, reaction time, sleep quality, and cognitive function. All of which are vital in the overall development of the adolescent.

NCT ID: NCT04261374 Completed - Dehydration Clinical Trials

Microcirculation in Dehydrated Older Patients

MicroCirc
Start date: June 1, 2019
Phase:
Study type: Observational

This proof-of-concept study examines whether 1) sublingual measurement in dehydrated old patients is feasible, 2) frailty and incompliance in old, awake patients affects video-quality, 3) dehydration impacts microcirculation This prospective observational study includes clinically dehydrated patients aged ≥ 65 years, who have spontaneous circulation and access to the sublingual mucosa, immediately after admission. Dehydration will be assessed clinically. A sidestream dark field camera (SDF) will be used for measurement. Video-quality will be evaluated with MIQS (microcirculation image quality score). Both AVA 4.3C- and AVA POEM-software analyzed the videos. Seventeen patients ≥ 65 years not showing dehydration served as control.

NCT ID: NCT04233606 Withdrawn - Clinical trials for Body Water Dehydration

Influence of Osmotic Stimulation of Vasopressin on Autonomic Function

Start date: November 2023
Phase: N/A
Study type: Interventional

The regulation of total body water that defines human hydration status is a complex and dynamic process. Current methods of assessing hydration status (e.g. hematologic and urinary analyses) lack the ability to track changes in hydration status in real-time due to whole-body homeostatic physiologic processes required to maintain central pressure and cardiovascular function. This project will address this problem by assessing the relationship between autonomic function (measured using heart rate variability), a brain-derived process that regulates cardiovascular function, and changes in the hydration-mediated hormone vasopressin.

NCT ID: NCT04155372 Not yet recruiting - Dehydration Clinical Trials

Effect of Different Fluid Ingestion Rate on Post-exercise Rehydration

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

The purpose of the present study is to investigate the effect of different rate of fluid consumption on post-exercise rehydration.

NCT ID: NCT04079543 Not yet recruiting - Clinical trials for Patient Satisfaction

NPO and Patient Satisfaction in the Cath Lab

FAST
Start date: September 9, 2019
Phase: N/A
Study type: Interventional

The purpose of this randomized, control study is to compare liberal vs strict nil per os (NPO) policies on patients undergoing transcatheter aortic valve replacement (TAVR) or arrhythmia ablation. The primary objective of this study is to determine if allowing clear liquids up to 2 hours prior to elective TAVR or elective arrhythmia ablation procedure improves patient satisfaction.