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Renal Insufficiency, Chronic clinical trials

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NCT ID: NCT03127852 Completed - Heart Failure Clinical Trials

Effects of Remote Patient Monitoring on Chronic Disease Management

Start date: August 23, 2016
Phase: N/A
Study type: Interventional

Remote patient monitoring is a potential component for the management of chronic conditions that may provide reliable and real-time physiological measurements for clinical decision support, alerting, and patient self-management. The purpose of this study is to evaluate an UHN-built remote monitoring system for patients with complex chronic conditions called Medly.

NCT ID: NCT03126318 Completed - Clinical trials for Chronic Kidney Diseases

A Study of Patients With Chronic Kidney Disease to Assess the Safety of a Single Dose of COR-001

COR-001-SC1
Start date: May 19, 2017
Phase: Phase 1
Study type: Interventional

This is a randomized, double-blind, placebo-controlled trial designed to evaluate the safety, pharmacokinetics, and pharmacodynamic effects of a single dose of the study drug or placebo administered subcutaneously to patients with moderate-to-severe chronic kidney disease and persistent inflammation.

NCT ID: NCT03125265 Completed - Clinical trials for End Stage Renal Disease

DIETary Intake, Death and Hospitalization in Adult With End-stage Kidney Disease Treated With HemoDialysis (DIET-HD) Study

Start date: January 5, 2014
Phase: N/A
Study type: Observational

The DIETary intake, death and hospitalisation in adults with end-stage kidney disease treated with HaemoDialysis (DIET-HD) study is a multinational prospective cohort study designed to evaluate the association between nutrition and dietary patterns and health outcomes in prevalent adult haemodialysis patients in Europe and South America.

NCT ID: NCT03121053 Recruiting - Clinical trials for Chronic Kidney Disease

Preventing contrAst Induced Nephropathy After TranscathEter Aortic Valve Replacement

PANTER
Start date: October 2016
Phase: Phase 4
Study type: Interventional

Chronic kidney disease (CKD) and (subsequent) acute kidney injury are frequent in patients undergoing transcatheter aortic valve implantation (TAVI). Moreover, these patients are easily hypervolemic and susceptible for cardiac decompensation. Prevention of contrast induced nephropathy (CIN) has not yet been studied in these patients, and evidence on different strategies is urgently needed. The objective of this study is to evaluate the efficacy of 250ml 1.4% sodium bicarbonate versus hypotone saline (0.65% sodiumchloride) hydration prior to TAVI in patients with CKD to prevent CIN.

NCT ID: NCT03120416 Completed - Clinical trials for Chronic Kidney Disease

Resistance Exercise Training in Chronic Kidney Disease

Start date: January 25, 2017
Phase: N/A
Study type: Interventional

The investigators aim to evaluate the feasibility of a resistance exercise training program among individuals with CKD and its impact on endothelial and vascular function.

NCT ID: NCT03119662 Terminated - Clinical trials for Chronic Kidney Diseases

A Study to Explore the Renal Safety of Visipaque Injection 320 mgI/mL in Patients With Chronic Kidney Disease

Start date: February 8, 2018
Phase: Phase 4
Study type: Interventional

This parallel-group, randomized, placebo-controlled study will examine the incidence and severity of acute kidney injury (AKI) in patients with chronic kidney disease (CKD) stage III/IV following an i.v. injection of iso-osmolar iodinated contrast material iodixanol (Visipaque™ Injection 320 mgI/mL), as compared with patients who received saline and underwent a non-enhanced CT (NECT) and duplex ultrasound (US) during their scheduled post-EVAR surveillance imaging.

NCT ID: NCT03108222 Active, not recruiting - Clinical trials for Chronic Kidney Disease Mineral and Bone Disorder

Phosphorus Absorption in Healthy Adults and in Patients With Moderate Chronic Kidney Disease

Start date: April 25, 2018
Phase:
Study type: Observational

Chronic kidney disease (CKD) affects approximately 26 million Americans with many more at risk for disease development. Elevated serum phosphorus (P) and related abnormalities in P homeostasis due to progressive loss of kidney function are primary driving forces behind cardiovascular dysfunction and mortality in CKD patients. Intestinal P absorption is an critical aspect in P homeostasis but has been understudied, particularly in the early stages of CKD progression. This study aims to determine P absorption in patients with moderate CKD compared to healthy adults.

NCT ID: NCT03106298 Completed - Clinical trials for Chronic Kidney Diseases

Iron Deficiency and FGF23 Regulation in CKD and HF

INDIGO
Start date: December 18, 2015
Phase:
Study type: Observational

This study investigates the effects of intravenous (IV) iron sucrose therapy on blood levels of Fibroblast Growth Factor 23 (FGF23, a protein that regulates the amount of phosphate in the body) in iron deficiency anemia in healthy participants, participants with Congestive Heart Failure (CHF, where the heart does not pump adequate blood supply to the body), participants with Chronic Kidney Disease (CKD, where the kidney function is reduced), and participants with CKD and CHF.

NCT ID: NCT03105817 Completed - Clinical trials for Chronic Kidney Disease Requiring Chronic Dialysis

Cellulose Triacetate Dialyzer in Hemodiafiltration-online

Start date: February 1, 2016
Phase: N/A
Study type: Interventional

In post-dilution haemodiafiltration only synthetic membranes have been used to date. The allergy problems described with these membranes require the development of other membranes capable of performing this treatment. We describe in vivo performance and behaviour of an asymmetric cellulose triacetate(ATA™) membrane, to identify its depurative effectiveness and ease of use in clinical practice, as well as evaluate its biocompatibility in a single haemodialysis session (acute biocompatibility) and after one month of treatment (chronic).

NCT ID: NCT03105271 Completed - Sickle Cell Disease Clinical Trials

Acute Kidney Injury in Patients With Sickle Cell Disease

Start date: January 1, 2017
Phase:
Study type: Observational

Patients with sickle cell disease may be at risk for acute kidney injury (AKI)during sickle cell crisis (pain or acute chest syndrome). This study will evaluate the role of hemolysis during SCD crisis on the development of AKI and the role for monitoring urine biomarkers during an admission for crisis and during well clinic follow-up.