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Renal Insufficiency, Chronic clinical trials

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NCT ID: NCT02232997 Completed - Clinical trials for Chronic Kidney Disease

Simplified Rapid Hydration in Preventing CA-AKI Among Patients With Chronic Kidney Disease

TIME
Start date: April 2015
Phase: N/A
Study type: Interventional

No well-defined protocols exist to guide fluid administration for prevention of contrast-associated acute kidney injury in high risk patients. The investigators will compare long term hydration at routine speed(12h before and after procedure at 1ml/kg/h) with short term hydration at high speed(1h before and 4h after procedure at 3ml/kg/h) to verify our hypothesis that the short term hydration may not be inferior to the long one.

NCT ID: NCT02232906 Completed - Iron Deficiency Clinical Trials

Switch From Oral Iron to Intravenous Ferric Carboxymaltose in Non-dialysis Chronic Kidney Disease (CKD)

Start date: March 2011
Phase: Phase 4
Study type: Interventional

Investigation whether a switch from oral iron to intravenous ferric carboxymaltose can reduce dose requirements of erythropoiesis-stimulating agents (ESA) and improve Hb levels and iron status in adult patients with non-dialysis-dependent CKD who were on a stable ESA/oral iron schedule for 6 months prior to enrolment.

NCT ID: NCT02232763 Completed - Proteinuria Clinical Trials

Efficacy and Safety of Losartan in Pediatric Chronic Kidney Disease With Tubular Proteinuria

Start date: September 2014
Phase: Phase 3
Study type: Interventional

The investigators hypothesize that using Losartan would help decrease proteinuria in pediatric chronic kidney disease with tubular proteinuria.

NCT ID: NCT02231138 Active, not recruiting - Clinical trials for Chronic Kidney Disease

Efficacy and Safety of Abelmoschus Manihot for Chronic Kidney Disease

Start date: September 2014
Phase: Phase 4
Study type: Interventional

Huangkui Capsule is a single medicament of traditional Chinese medicine consists of Abelmoschus manihot and has been widely used to treat kidney disease. The purpose of this study is to evaluate the safety and efficacy of Abelmoschus manihot for treating chronic kidney disease in large scale samples with long time take.

NCT ID: NCT02230202 Completed - Clinical trials for Chronic Kidney Disease

Endothelial Microparticles: A Novel Marker of Vascular Dysfunction

Start date: September 2014
Phase: N/A
Study type: Observational [Patient Registry]

The primary hypothesis of this proposal is that chronic kidney disease (CKD) and treatment with calcineurin inhibitors (CNIs) are each associated with the release of endothelial microparticles into the plasma.

NCT ID: NCT02229435 Completed - Clinical trials for Chronic Kidney Disease (CKD)

Urologic-nephrological Care of Chronic Kidney Disease in Saxony-Anhalt/Magdeburg.

UroCKDisS
Start date: December 2004
Phase: N/A
Study type: Observational [Patient Registry]

Statement: Patients with Chronic kidney disease (CKD) with an estimated glomerular filtration rate (eGFR) under 60 ml/min using the MDRD-6 (Modification of Diet in Renal Disease) formula and/or CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration) formula should undergo nephrological and urological care (diagnosis and treatment) to prevent chronic kidney failure. This is recommended by the National Kidney Foundation Kidney Disease Outcomes Quality Initiative (KDOQI), Kidney Disease Improving Global Outcomes (KDIGO) and European Urological Association (EAU). Renal and postrenal diseases can cause or worsen CKD. Internistic and intrarenal diseases can caused or worsen CKD. All diseases affecting CKD should be treated and the medical care should be optimized. Hypothesis: Not all patients with CKD receive urological and nephrological care. Interdisciplinary work of outpatient working urologists and nephrologists in the metropolitan area Magdeburg / Saxony-Anhalt Germany is unknown. An descriptive analysis of interdisciplinary treatment connection of CKD patients for an orientating statement is needed.

NCT ID: NCT02228655 Terminated - Clinical trials for Anemia in Chronic Kidney Disease

An Exploratory Study to Evaluate FMX-8 to Treat Anemia in CKD

Start date: October 2014
Phase: Phase 0
Study type: Interventional

FMX-8 is a new type of drug being tested for the treatment of anemia in chronic illnesses.

NCT ID: NCT02224820 Completed - Clinical trials for Chronic Kidney Disease

Phase II Study to Evaluate Safety and Efficacy of Intravenous Immunoglobulin G Degrading Enzyme of Streptococcus Pyogenes (IdeS) in Chronic Kidney Disease

Start date: June 2014
Phase: Phase 2
Study type: Interventional

IdeS is an immunoglobulin g (IgG) cleaving enzyme. It will given to patients with donor specific antibodies to reduce the antibody load and thus enable kidney transplantation. IdeS antibody reducing efficacy and its safety will be studied.

NCT ID: NCT02222402 Completed - Clinical trials for End-Stage Kidney Disease

PrEscription of Intra-Dialytic Exercise to Improve quAlity of Life in Patients With Chronic Kidney Disease

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

The PEDAL study aims to evaluate the effectiveness of a 9-month intradialytic exercise training intervention designed to improve quality of life (QOL) and alleviate functional limitations in patients with stage 5 Chronic Kidney Disease (CKD) who are on haemodialysis. Exercise rehabilitation will be compared against established treatment options available within UK NHS haemodialysis (HD) units. A qualitative substudy will also investigate the experience and acceptability of the intervention for both participants and members of the renal care team. In addition, we want to examine whether this type of additional exercise treatment is cost effective within the health service setting. PEDAL is designed as a multi centre randomised clinical trial (RCT) and will recruit 380 adult patients who have been on HD for at least 3 months, from 10 HD sites located in Scotland, England and Wales. The type of exercise programming will consist of cycling exercise performed during each dialysis session plus a muscle conditioning programme performed twice per week. All exercise sessions will be supervised by a physiotherapy assistant. The exercise prescription will be individualised for all patients on the basis of their fitness and clinical status. The main objective is to examine the impact of exercise rehabilitation on quality of life and well being of patients. We hypothesise that the exercise training delivered during haemodialysis treatment will significantly improve the functional limitations/abilities of the patients leading to the detection of clinically beneficial improvement in quality of life outcome, as measured by the KDQOL-36 physical composite score (PCS) at the primary end point.

NCT ID: NCT02218099 Completed - Healthy Subjects Clinical Trials

A Study to Evaluate the Pharmacokinetics, Pharmacodynamics and Safety of ASP8232 in Subjects With Renal Impairment and in Type 2 Diabetes Mellitus Subjects With Chronic Kidney Disease

Start date: September 16, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This study consists of two parts. Part 1 evaluates the effect of renal impairment on the PK and PD of a single dose of ASP8232. In addition, the safety and tolerability will be assessed. Part 2 evaluates the PK, PD, and safety and tolerability of multiple doses of ASP8232 compared with placebo in Type 2 Diabetes Mellitus (T2DM) subjects with Chronic Kidney Disease (CKD).