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Renal Insufficiency, Chronic clinical trials

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NCT ID: NCT02358967 Completed - Clinical trials for Chronic Kidney Disease

Palm Tocotrienols in Chronic Hemodialysis (USA)

PATCH
Start date: June 15, 2017
Phase: N/A
Study type: Interventional

Patients undergoing chronic hemodialysis are at increased risk for cardiovascular disease, attributed in part to increased oxidative stress, inflammation and dyslipidemia. Intervention with a naturally occurring dietary supplement may improve certain biomarkers of inflammation and oxidative stress and improve the lipid profile.

NCT ID: NCT02358096 Completed - Type 2 Diabetes Clinical Trials

A Study to Evaluate ASP8232 as Add-On Therapy to Angiotensin Converting Enzyme Inhibitor (ACEi) or Angiotensin Receptor Blocker (ARB) in Reducing Albuminuria in Patients With Type 2 Diabetes and Chronic Kidney Disease

ALBUM
Start date: March 17, 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of ASP8232 in reducing Urinary Albumin to Creatinine Ratio (UACR) in subjects with Type 2 Diabetes Mellitus (T2DM) and Chronic Kidney Disease (CKD) at 12 weeks compared to placebo.

NCT ID: NCT02357199 Completed - Clinical trials for Renal Insufficiency, Chronic

Interventional Study Targeting Oral Infections in Patients With Chronic Kidney Disease

Start date: January 2015
Phase: N/A
Study type: Interventional

This study aims to investigate the prevalence of oral infection in chronic renal disease patients and to examine whether a focused oral hygiene intervention can reduce oral infection leading to reduced systemic inflammatory parameters in chronic renal disease patients in hemodialysis, chronic renal disease patients waiting for kidney transplantation, and chronic renal disease patients who has been transplanted 1-1½ year previously. The results will be compared to a gender- and age-matched healthy control group.

NCT ID: NCT02351349 Completed - Clinical trials for Chronic Kidney Disease

Chronic Kidney Disease Among Frail Elderly

FRED-CKD
Start date: January 2016
Phase: N/A
Study type: Interventional

Chronic kidney disease is a common diagnosis in the elderly population and it is associated with significant morbidity and health care costs. The prevalence rates increase with age to about 40% for adults aged > 65 years. In the elderly population (age 65 and over), CKD is associated with a higher burden of comorbid conditions and frailty. The prevalence of frailty is higher in CKD patients with rated being double in early stages and nearly 6 times higher beyond stage 3b. Previously reported frailty mortality rates of 18% at 3 years and 47% at 7 years comparing with mortality rates in non frail individuals of 3% and 12% respectively. In this study, the investigators investigate the effect of multidisciplinary interventions upon frail elderly patients with CKD not yet on dialysis. This interventions include best medical care, nutrition, physiotherapy, and social, psychological and spiritual support.

NCT ID: NCT02348996 Completed - Clinical trials for Chronic Kidney Disease

Study Comparing Dryweight Determination in Hemodialysis Patients With Two Methods

Start date: February 2014
Phase: N/A
Study type: Interventional

Adequate control of extracellular volume is a major goal of renal replacement therapy in patients with chronic renal disease. Fluid overload is present in the early stages of chronic kidney disease and contributes significantly to hypertension, arteriosclerosis and high prevalence of left ventricular hypertrophy. These are associated with high rates of morbidity and mortality in this group of patients, rates on dialysis in Brazil is around17.9 % per year. Dry weight during hemodialysis remains a delicate gap between hypervolemia and hypovolemic. Many studies have shown that tight control of post - dialysis weight is related to better outcomes in short term and higher long-term survival. Many methods have been proposed for estimating the hydration status of hemodialysis patients in an objective manner, including ultrasonography of the inferior vena cava and echocardiography. However, these methods are very time-consuming and cumbersome to use in daily practice. In most dialysis centers, the dry weight is evaluated on subjective clinical criteria, with trial and error and time consuming. It was recently introduced in Brazil to monitor body composition by multifrequency bioimpedance, called Body Composition Monitor ( BCM ) manufactured by Fresenius Medical Care. The BCM is a piece of bioimpedance spectrometry using a three compartment model, able to quantify objectively and accurately the extracellular volume and hydration status of each patient by measuring body resistance to an electric current. The procedure is safe, simple and relatively inexpensive. The BCM uses multi-frequency currents (ranging from 5 to 1000 KHz ). The availability of this device evaluation of body composition which assesses the dry weight more efficiently and objectively determine a target to be achieved to prevent left ventricular hypertrophy, hypertension better manage and improve cardiovascular outcomes, motivates us to perform this study. So the goal is to compare the efficacy between bioelectrical impedance analysis and clinical evaluation for suitability of dry weight in hemodialysis patients. A prospective, randomized, crossover study, which will include all chronic renal failure patients on hemodialysis at St. Luke 's Hospital (PUC - RS), including patients with at least three months on HD and over 18 years of age. The expected primary outcome is to achieve greater accuracy in determining the state of hydration and dry weight of these patients.

NCT ID: NCT02342639 Completed - Clinical trials for Chronic Kidney Disease

Rifaximin Therapy in Chronic Kidney Disease

Start date: June 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if Rifaximin decreases serum and urine levels of bacterial byproducts and inflammatory markers in patients with chronic kidney disease and to evaluate changes in the bacterial content of the stool from these individuals.

NCT ID: NCT02341885 Completed - Acute Kidney Injury Clinical Trials

PrEvalence of Acute and Chronic Kidney Disease Treated by Renal Replacement Therapy

PEACE
Start date: March 2015
Phase: N/A
Study type: Observational

A prospective international, multi-centre, prevalence study on the epidemiology of the use of renal replacement therapy for ICU patients who have acute kidney injury and chronic end stage kidney disease.

NCT ID: NCT02341664 Completed - Stroke Clinical Trials

Patient and Provider Assessment of Lipid Management Registry

PALM
Start date: May 2015
Phase:
Study type: Observational [Patient Registry]

The purpose of the Patient and Provider Assessment of Lipid Management Registry (PALM) is to gain a better understanding of physicians' cholesterol medication prescribing practices, patient and physician attitudes and beliefs related to cholesterol management, and current utilization of cholesterol-lowering therapies given the new ACC/AHA guideline recommendations. The PALM Registry hopes to allow for the design of ways to improve cholesterol management and decrease the burden of cardiovascular disease (CVD) in the US.

NCT ID: NCT02341417 Completed - Clinical trials for Secondary Hyperparathyroidism, Chronic Kidney Disease

Extension Study of Cinacalcet for Treatment of Secondary Hyperparathyroidism (SHPT) in Pediatric Patients With Chronic Kidney Disease on Dialysis

Start date: June 10, 2015
Phase: Phase 3
Study type: Interventional

The primary objective of this study was to characterize the long-term safety and tolerability of cinacalcet in pediatric patients with chronic kidney disease (CKD) receiving dialysis.

NCT ID: NCT02338323 Completed - Clinical trials for Chronic Kidney Disease

Compare the Renal Protective Effects of Febuxostat and Benzbromarone

Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether febuxostat and benzbromarone could protect renal function, and which one could be better.