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Complication of Hemodialysis clinical trials

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NCT ID: NCT02950389 Completed - Clinical trials for Complication of Hemodialysis

REmoval of Free Light Chains. A COmpaRison of Three Different dialyzERs

RECORDER
Start date: January 2016
Phase: N/A
Study type: Interventional

Immunoglobulin light chains are classified as middle molecule uremic toxins able to interact with B lymphocyte membranes leading to the activation of transmembrane signaling. The ensuing impairment of neutrophil function can contribute to the chronic inflammation state of uremic patients, and the increased risk of bacterial infections or vascular calcifications. The aim of this crossover observational study was to assess the difference in free light chain removal by three different hemodialysis filters in patients not affected by multiple myeloma. Free light chain removal was compared in the polymethylmethacrylate (PMMA) membrane Filtryzer BK-F, the polyphenylene HFR17 filter and the conventional polysulfone filter F7 High Performance dialysers (HPS). Twenty chronic hemodialysis patients were enrolled. The patients were randomized into two groups of treatment lasting six weeks each. The dialysis sessions checked were the midweek sessions and the blood was drawn at times 0, 120' and 240'. Kappa (k) and lambda (l) light chain levels, beta2microglobulin (β2M), C reactive protein (CRP) and albumin were checked.

NCT ID: NCT02870829 Completed - Clinical trials for Vascular Calcification

Treatment to Reduce Vascular Calcification in Hemodialysis Patients Using Vitamin K

TReVasc-HDK
Start date: July 2016
Phase: Phase 2
Study type: Interventional

The proposed study will seek to evaluate the prevalence and the progression of vascular calcification in a cohort of maintenance hemodialysis patients in Asian population. It will also evaluate the efficacy of vitamin K 2 supplementation in reducing the progression of vascular calcification in this group of patients. This will be a single-center randomized, prospective and open-label interventional clinical trial of end stage renal failure patients on hemodialysis.Primary outcome will be absolute difference in coronary artery calcium (CAC) score at 18-month between control and intervention arms. Secondary outcomes will be to compare absolute difference in aortic valve calcification, percentage of patients with regression of coronary artery calcification of at least 10%, absolute difference in aortic and systemic arterial stiffness, mortality from any cause and major adverse cardiovascular events (MACE) over the same period.

NCT ID: NCT02747966 Completed - Clinical trials for Complication of Hemodialysis

The Relationship Between the Flow of Arteriovenous Fistula and Cardiac Function in Haemodialysis Patients

Start date: April 2009
Phase: N/A
Study type: Observational

A prospective longitudinal surveillance for a period of 2 months. Sample - identify suitable Chronic Kidney Disease (CKD) patients who undergo HD with functioning AVF. Participants at various age range and both sexes are recruited to observe their access flow, access recirculation and cardiac function and assess their relationship.

NCT ID: NCT02558153 Completed - Clinical trials for Vascular Access Complication

RCT of Paclitaxel DEB Compared to Standard PTA in Dialysis Fistula

APERTO
Start date: June 2015
Phase: N/A
Study type: Interventional

A multicenter randomized clinical trial of paclitaxel drug-eluting balloon (DEB) versus standard percutaneous transluminal angioplasty (PTA) to reduce restenosis in 150 patients with haemodialysis access stenoses.

NCT ID: NCT02513303 Completed - Clinical trials for End Stage Renal Disease

Trial to Evaluate the Sirolimus-Eluting Collagen Implant on AV Fistula Outcomes

ACCESS
Start date: November 2015
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate efficacy and safety outcomes following use of the Sirolimus-eluting Collagen Implant (SeCI) in subjects undergoing surgical creation of an AV fistula for vascular access (index procedure).

NCT ID: NCT02443376 Completed - Clinical trials for Complication of Hemodialysis

The Effects of Hemodialysis Session on Vascular Stiffness

PWV/CP/HD
Start date: May 2015
Phase: N/A
Study type: Observational

Central blood pressure and pulse wave velocity were measured using a Complior Analyse device before and immediately after the end of the dialysis session.

NCT ID: NCT01825590 Completed - Clinical trials for Complication of Hemodialysis

Effects of Simple Sodium Alignment on Clinical Outcomes

Start date: May 2011
Phase: N/A
Study type: Observational

A difference between dialysate and serum sodium concentration leads to diffusive sodium transfer across the dialyzer membrane. The consequences of diffusive sodium flux into the patient can be chronic sodium overload leading to overhydration, hypertension, cardiovascular disease, and other problems. Diffusive sodium flux out of the patient can lead to intradialytic blood pressure instability. A simple strategy for alignment of dialysate and serum sodium concentrations was implemented starting in April/May 2010 in order to minimize the problems particularly associated with chronic sodium overload.

NCT ID: NCT01396980 Completed - Clinical trials for Complication of Hemodialysis

Microcirculation During Haemodialysis

Start date: September 2011
Phase: N/A
Study type: Observational

- SDF is validated by measuring changes in microcirculation in sepsis patients with MOF (Boerma studies). - SDF is validated by measuring changes in microcirculation in stable chronic hemodialysis patients (NDT 2009 Bemelmans). - Ultrafiltration in stable chronic hemodialysis leads to a decrease in sublingual microcirculatory flow (NDT 2009 Bemelmans). - Trendelenburg position improves the sublingual microcirculatory flow at the end of hemodialysis treatment (NDT 2009 Bemelmans). - Hemodialysis with ultrafiltration leads to a significant reduction of myocardial perfusion and cardiac output (NDT 2009 Dasselaar) - Cardiac output measurement during dialysis is not practical. - BVM is a validated method for hypotension due to ultrafiltration to prevent the amount of ultrafiltration online change based on the measured haemoconcentration (ref Dasselaar et al NDT 2005). - BCM is a validated measurement to the dry weight in hemodialysis patients measured by a bioimpedance technique (NDT Passauer et al 2009).

NCT ID: NCT01278693 Completed - Clinical trials for Complication of Hemodialysis

Effect of Oral L-carnitine Supplement on Lipid Profile, Anemia, and Quality of Life of Patients

Start date: August 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine Effect of oral L-carnitine supplement on lipid profile, anemia, and quality of life.

NCT ID: NCT01147354 Completed - Inflammation Clinical Trials

Effect of Selenium Supplementation on Inflammatory,Oxidative and Nutritional Markers in Hemodialysis Patients

Start date: April 2009
Phase: Phase 3
Study type: Interventional

The aim of this study is to evaluate the effect of selenium supplementation on oxidative, inflammatory and nutritional markers in hemodialysis patients.