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Renal Insufficiency, Chronic clinical trials

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NCT ID: NCT01353417 Completed - Clinical trials for Chronic Kidney Insufficiency

Non-interventional-study With Tacrolimus Sandoz© Capsules for Prophylaxis of Renal Graft Rejection

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

This non-interventional study intends to collect epidemiological data in patients with stable kidney function after renal transplantation, who receive Tacrolimus Sandoz© according to the approved indication.

NCT ID: NCT01351636 Completed - Clinical trials for Chronic Kidney Disease

Effect of Arotinolol Hydrochloride on Cardiovascular Events in Hypertensive Haemodialysis Patients

AHOCEP
Start date: April 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to ascertain whether Arotinolol Hydrochloride reduces mortality and cardiovascular events in chronic kidney disease stage 5 patients with hypertension.

NCT ID: NCT01350388 Completed - Diabetes Clinical Trials

Effects of Febuxostat on Adipokines and Kidney Disease in Diabetic Chronic Kidney Disease

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

Hyperuricemia is emerging as a risk factor for development of diabetes and metabolic syndrome. Recently, it was shown in in-vitro cell culture experiments that hyperuricemia induces redox-dependent signaling and oxidative stress in adipocytes. By targeting levels of uric acid with febuxostat we hypothesize that the levels of oxidative stress in adipose tissue (obtained by fat biopsy) will decrease. Primary aims of the study is to determine whether febuxostat therapy in overweight or obese, diabetic patients with stage 3 CKD and high serum uric acid levels 1. decreases adipose tissue concentrations of thiobarbituric acid reactive substance (TBARS), a marker of oxidative stress 2. increases adipose tissue expression and concentrations of adiponectin and 3. decreases urinary concentrations of transforming growth factor (TGF)- B1.

NCT ID: NCT01345656 Completed - Heart Failure Clinical Trials

BAY94-8862 Dose Finding Trial in Subjects With Chronic Heart Failure and Mild (Part A) or Moderate (Part B) Chronic Kidney Disease

ARTS
Start date: May 9, 2011
Phase: Phase 2
Study type: Interventional

A placebo (Part A) and placebo and active comparator controlled (Part B), double-blind and randomized study to assess safety and tolerability of a new drug (BAY94-8862) given orally

NCT ID: NCT01342263 Completed - Heart Failure Clinical Trials

Trial of an Internet-based Platform for Managing Chronic Diseases at a Distance

iCDM
Start date: May 2011
Phase: N/A
Study type: Interventional

In 2005, more then one-third of Canadians were burdened with one or more chronic diseases. Patients with one chronic disease often have, or are at risk for, another chronic disease. This group of complex patients represents a substantial challenge to healthcare resources. For patients in rural communities, the opportunity to attend ambulatory care clinics is not always an option. Additionally, the opportunity for rural patients to receive quality care close to, or within their homes, is of great benefit as it reduces the need for extensive travel and the potential burden of clinical visits. The use of telehealth has been identified as an effective modality for chronic disease management and is actively promoted by national organizations as having great promise for health service delivery in rural areas. The Internet as a mode for healthcare delivery has numerous advantages: 1. it is ubiquitous with increasing access in all age groups, 2. it is inexpensive, 3. it facilitates both patient data transfer and patient feedback, thereby supporting patient self-management, 4. it is scalable to large patient volumes, 5. it delivers health care directly to the patient and 6. it requires minimal set-up for patients with current Internet access. The investigators propose to develop and evaluate a multi-chronic disease management program delivered through the Internet (with telephone supports) focused on high-impact chronic diseases targeted to patients in rural communities. This study will consist of a single-blinded randomized controlled trial to investigate the efficacy of the iCDM in 318 patients with two or more of the target chronic diseases living in rural areas. Within this Aim, the investigators will be able to address the following research questions: Q1. What is the effect of iCDM on healthcare utilization and patient self-management outcomes? Q2. What is the long-term compliance to the iCDM? Q3. What is the level of patient and provider satisfaction?

NCT ID: NCT01341782 Completed - Hemodialysis Clinical Trials

Comparison of Efficacy and Safety of Paricalcitol Injection With Maxacalcitol Injection in Adult Japanese Chronic Kidney Disease Subjects Receiving Hemodialysis With Secondary Hyperparathyroidism

Start date: May 2011
Phase: Phase 3
Study type: Interventional

This study is a comparison of the efficacy and safety of paricalcitol injection with maxacalcitol injection in adult Japanese chronic kidney disease patients receiving hemodialysis with secondary hyperparathyroidism. The main objective of this study is to demonstrate the efficacy of paricalcitol injection in reducing levels of parathyroid hormone without clinically significant hypercalcemia, compared to maxacalcitol injection.

NCT ID: NCT01341691 Completed - Clinical trials for Chronic Kidney Disease

Phosphate Binding of Chitosan Chewing Gum in Patients With Chronic Kidney Disease (CKD)

Start date: March 2011
Phase: Phase 0
Study type: Interventional

To determine the amount of phosphate recovered into 2 strengths of K2CG chewing gum in a modified formulation (with or without an extender) added to the gum core, in comparison to matching placebo gums.

NCT ID: NCT01341678 Completed - Clinical trials for Chronic Kidney Disease

Circadian Rhythm Modulation by Dietary Phosphorus in Chronic Kidney Disease

Start date: April 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to describe the circadian rhythm of serum and salivary phosphorus in patients with chronic kidney disease and determine its' modification in response to changes in dietary phosphate load.

NCT ID: NCT01336140 Completed - Clinical trials for Patients With Severe Chronic Kidney Disease Being Evaluated With Nuclear Stress Testing of the Heart Using the Stress Agent Regadenoson

Attenuation of the Side Effect Profile of Regadenoson: Study With Aminophylline in Patients With Severe Kidney Disease Undergoing Myocardial Perfusion Imaging

ASSUAGE-CKD
Start date: June 2011
Phase: Phase 4
Study type: Interventional

The routine administration of 75 mg of intravenous aminophylline in patients with severe chronic kidney disease undergoing a nuclear stress test with regadenoson (Lexiscan®) can reduce or eliminate the incidence of diarrhea and other side effects related to regadenoson.

NCT ID: NCT01328470 Completed - Clinical trials for Chronic Kidney Disease

Effect of Platelet Inhibition According to Clopidogrel Dose in Patients With Chronic Kidney Disease

CKD
Start date: September 2009
Phase: Phase 4
Study type: Interventional

Impaired renal function is associated with reduced responsiveness to clopidogrel. There are no studies which have shown a means by which to overcome platelet hyporesponsiveness in patients with chronic kidney disease (CKD). The purpose of this study was to determine the functional impact of cilostazol in patients with CKD undergoing hemodialysis.