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Renal Insufficiency clinical trials

View clinical trials related to Renal Insufficiency.

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NCT ID: NCT02427035 Completed - Clinical trials for Acute Myocardial Infarction

A Study of CSL112 in Healthy Adults and in Adults With Moderate Renal Impairment

Start date: May 2015
Phase: Phase 1
Study type: Interventional

This is a phase 1 multicenter, randomized, double-blind, placebo-controlled, ascending dose study to investigate the pharmacokinetics (PK), safety, and tolerability of CSL112 in adult subjects with moderate renal impairment and in healthy adult subjects with normal renal function.

NCT ID: NCT02424851 Completed - Multiple Myeloma Clinical Trials

Optimising Renal Outcome in Myeloma Renal Failure

OPTIMAL
Start date: November 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the effectiveness of bortezomib versus thalidomide in reducing free light chains in the blood of myeloma patients. In addition participants will receive bendamustine (chemotherapy) and dexamethasone (steroids), which increase the effectiveness of both bortezomib and thalidomide. The trial will also study whether an earlier reduction of free light chains increases the chances of the kidneys recovering.

NCT ID: NCT02420184 Completed - Clinical trials for Sleep Apnea, Obstructive

Treatment of Obstructive Sleep Apnea in Chronic Kidney Disease

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

This study is being conducted to determine whether treatment of obstructive sleep apnea (OSA) in patients with chronic kidney disease (CKD) improves kidney function. Half of the participants will receive continuous positive airway pressure (CPAP) treatment for their OSA in addition to their regular CKD treatment, while the other half will only receive their regular CKD treatment.

NCT ID: NCT02420119 Completed - Clinical trials for Chronic Renal Failure

Does Intravenous Iron Therapy Decrease Serum Phosphorous Levels?

Start date: January 2015
Phase:
Study type: Observational

Intravenous iron therapy is common and effective, with few side effects. Two formulations are used, venofer or iron sucrose and ferrlecit, or ferric gluconate. The association between intravenous iron use and decrease in serum phosphorus and vitamin D levels, with increased fractional excretion of phosphorus, has been observed with older iron preparations, such as saccharated ferric oxide. However, hypophosphatemia and osteomalacia have been reported with iron carboxymaltose, a newer iron formulation. There is no information in the literature about phosphorus and vitamin D levels after treatment with venofer or ferrlecit. We intend to check phosphorus and vitamin D serum levels in our patients prior to and after treatment with these iron formulations.

NCT ID: NCT02418065 Recruiting - Clinical trials for Chronic Kidney Failure

Multimodal Therapeutic Approach in Undernourished Maintenance Hemodialysis Patients (AMERICANO)

AMERICANO
Start date: December 2013
Phase: Phase 3
Study type: Interventional

The aim of the study is to evaluate a 3 months integrated multimodal therapeutic approach including exercise training program with ergocycle during dialysis sessions, oral nutritional supplementation, omega 3 and androgen, on effort tolerance and quality of life of under-nourish maintenance hemodialysis Chronic Kidney Disease (CKD) patient.

NCT ID: NCT02417571 Active, not recruiting - Hypertension Clinical Trials

Effect of Ambulatory BP Monitoring on the CliniCal coUrse and RenAl ouTcomE of CKD

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

Control of blood pressure (BP) is the first thing to do in the management of chronic kidney disease (CKD). Although guidelines suggest the optimal blood pressure level, it is hard to assess BP correctly during the office visit. Often there is a discrepancy between office BP and out-of-office BP, including home BP and ambulatory BP. Recent study reported that as many as 34% of Korean CKD patients had masked hypertension, which means high BP by ambulatory BP monitoring but normal BP by conventional office BP measurement. This study aims to evaluate the effect of ambulatory BP-guided BP management on the clinical outcome of CKD, compared to the conventional management using office BP.

NCT ID: NCT02410642 Completed - Renal Impairment Clinical Trials

NAG-excretion During Cardiopulmonary Bypass

CPBNAG
Start date: November 2011
Phase: N/A
Study type: Observational

NAG is a protein excreted in urine in cases of tubular damage, and is considered a biomarker of kidney injury. Elevated urinary NAG is seen after cardiac surgery, but the clinical significance, pattern of excretion and links to perioperative factors are poorly described. We plan a study of the pattern of NAG-excretion during cardiac surgery with cardiopulmonary bypass, and explore possible associated variables.

NCT ID: NCT02405884 Completed - Glaucoma Clinical Trials

Intraocular Pressure and Hemodialysis Midwestern Brazil

EHPIOBRAZIL
Start date: January 2014
Phase: N/A
Study type: Interventional

Objective: To evaluate the variation in intraocular pressure in patients with chronic kidney disease, according to the time interval between hemodialysis sessions and to the influence of weight and blood pressure on intraocular pressure. Methods: This was a cross-sectional study in which 78 eyes of 39 patients on hemodialysis, at the Santa Casa de Misericordia de Goiânia hospital, were analyzed in June 2014. Patients were divided into groups according to the days on which they underwent hemodialysis. The mean, standard deviation, and median of the intraocular pressure, blood pressure, and weight were calculated. P-values <0.05 were considered statistically significant.

NCT ID: NCT02405650 Completed - Obesity Clinical Trials

CRIC-Visceral Adiposity and Physical Fitness in Chronic Kidney Disease

CRIC-VAP
Start date: April 2015
Phase:
Study type: Observational

Obesity and chronic kidney disease (CKD) are major public health problems. In contrary to observations in general population, higher body mass index in those with pre-existing CKD is associated with lower mortality. Chronic Renal Insufficiency Cohort (CRIC) is an ongoing observational study to examine the consequences of CKD with a particular focus on cardiovascular illness like myocardial infarction (heart attack) and stroke. Among CRIC study participants, the investigators propose to obtain visceral and subcutaneous adiposity and physical fitness measures and study its associations with patient-centered outcomes. This study will help the investigators understand the independent and combined effects of visceral adiposity and physical fitness on cardiovascular disease, renal disease progression and death among those with CKD. Further, it will identify mechanisms that could be targeted to reduce the detrimental effects of visceral adiposity in those with kidney disease.

NCT ID: NCT02405195 Completed - Renal Impairment Clinical Trials

Renal Perfusion, Filtration and Oxygenation During Cardiopulmonary Bypass (CPB)

ECCSTUD
Start date: October 2011
Phase:
Study type: Observational

Acute kidney injury is a common complication after cardiac surgery with cardiopulmonary bypass (CPB). This study aims to investigate the effects of CPB on renal perfusion, filtration and oxygenation.