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Renal Insufficiency clinical trials

View clinical trials related to Renal Insufficiency.

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NCT ID: NCT01229072 Suspended - Clinical trials for Chronic Renal Failure

Safe Use of Heparin Sodium in Patients With Chronic Renal Failure.

Heparin
Start date: July 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The Heparin form a complex with a plasma protein, antithrombin III (ATIII), which is an endogenous anticoagulant. This complex inhibits the formation of thrombin and accelerates its destruction. Moreover, heparin and other proteases ATIII inactivate the clotting cascade, especially the anti-activated factor X. The end result of these actions is the inhibition of biochemical training and synthesis of certain clotting factors that activators of critical functions in the genesis of a blood clot. Patients with chronic renal failure (CRF) who use the treatment of hemodialysis need a system of anticoagulation with the direct thrombin inhibitor and / or heparinóides to prevent thrombosis. Based on clinical studies, to control the level of plasma heparin in patients with CRF is essential. Evidence of clotting as APTT, TP, ACT and proof of the activity of anti-factor Xa should be used as a substrate of protection for those patients on hemodialysis.

NCT ID: NCT01228643 Withdrawn - Clinical trials for Chronic Renal Failure

Effectiveness of Pancreatic Enzymes in Patients Pancreatic Insufficient: Comparison of Two Drugs

Start date: June 2007
Phase: Phase 3
Study type: Interventional

Prove the efficacy of pancreatic enzyme Norzyme ® imported by Pharmaceutical Chemistry Laboratory Bergamo Ltda. verified by activity lipase contained in the formulation in controlling steatorrhea in 16 patients of both sexes aged 14 to 65 years, patients with pancreatic insufficiency Exogenous any cause. It's effectiveness will be found in a study randomized, crossover, comparative biosimilar product produced by Creon ® Laboratory Solvay Farma Ltda.

NCT ID: NCT01228123 Completed - Acute Renal Failure Clinical Trials

Clinical Trial Comparing Continuous Versus Intermittent Hemodialysis in ICU Patients

CONVINT
Start date: January 2002
Phase: Phase 2/Phase 3
Study type: Interventional

The mortality of acute renal failure (ARF) remains to be high (around 60-70%) despite manifold improvements in ICU care. At present, it is not clear if the method chosen for renal replacement therapy, i.e. intermittent haemodialysis (IHD) or continuous haemofiltration (CVVH), might impact on the outcome of these patients. For this purpose, a prospective randomised clinical study of the effect of continuous versus intermittent renal replacement therapy on the mortality and outcome of acute renal failure will be performed.

NCT ID: NCT01227122 Recruiting - Clinical trials for Cardiac Surgical Procedures

NGAL Predictive Value of Acute Kidney Failure After Cardiac Surgery in Patients With Preoperative Chronic Kidney Failure

NGAL-CKF
Start date: August 2010
Phase: N/A
Study type: Observational

Primary endpoint: To evaluate predictive value of plasmatic levels of Neutrophil Gelatinase Associated Lipocalin (NGAL) to reveal acute kidney failure after cardiac surgery in patients with preoperative chronic kidney failure Secondary endpoint is to obtain threshold values of NGAL.

NCT ID: NCT01225458 Terminated - Aged Clinical Trials

Behaviour and Cognitive Evaluation for Dialysis Elderly Patients (BCDE)

BCDE
Start date: July 2008
Phase: N/A
Study type: Interventional

The trial is a multicenter, prospective, randomized, open study. A total of 500 elderly patients aged over 75 years with renal insufficiency stage 5 will be included in the study after signed informed consent. Patients will be randomized 1/1 in two arms : 250 patients in the "exclusive nephrology follow-up" arm will continue their usual follow-up; 250 patients in the "geriatric follow-up" arm will have both their usual nephrology follow-up and a geriatric follow-up. The aim of the study is to determine if a systematized gerontologist evaluation delay the occurrence of a composite primary endpoint : death, dementia, depression and severe dependency. The hypothesis is that the functional and vital prognosis of a patient with renal insufficiency depends not only on common and classical factors but also on cognitive and psychological functions and dependence, particularly in elderly patients.

NCT ID: NCT01223755 Terminated - Clinical trials for Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Sirolimus In Autosomal Dominant Polycystic Kidney Disease And Severe Renal Insufficiency

SIRENA-II
Start date: September 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The general aim of this study in adult patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and severe renal insufficiency is to assess the safety and the efficacy of sirolimus (SRL) in slowing renal function decline as compared to conventional therapy.

NCT ID: NCT01220843 Completed - Clinical trials for Chronic Renal Failure

FGF23 Reduction : Efficacy of a New Phosphate Binder in CHronic Kidney Disease

FRENCH
Start date: October 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate in Chronic Kidney Disease (CKD) patients not on dialysis and who have an Fibroblast growth factor 23 (FGF23) serum levels elevated, the effect of non calcic phosphate binder: sevelamer carbonate. This treatment could lead to a diminution of FGF23 serum levels due to the diminution of intestinal absorption of dietary phosphate. In addition, the investigators will describe the impact of the FGF23 level monitoring on the main phosphocalcium metabolism markers as phosphatemia, intact parathyroid hormone (iPTH), serum calcitriol and phosphaturia.

NCT ID: NCT01213914 Active, not recruiting - Burns Clinical Trials

Hemofiltration in Burns: RESCUE (Randomized Controlled Evaluation of Hemofiltration in Adult Burn Patients With Septic Shock and Acute Renal Failure)

RESCUE
Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this study is determine if High-Volume Hemofiltration in addition to 'contemporary' care will result in an improvement of select clinical outcomes when compared to 'contemporary' care alone in the treatment of critically ill patients with ARF secondary to septic shock.

NCT ID: NCT01213212 Completed - Diabetes Mellitus Clinical Trials

Preventing Renal Functional Abnormalities With Calorie Restriction in Subjects With Abdominal Obesity and Type 2 Diabetes at Increased Renal and Cardiovascular Risk

CRESO
Start date: September 2009
Phase: Phase 2
Study type: Interventional

The study investigates whether a caloric restricted dietary regime can prevent onset and/or progression of chronic kidney disease in type 2 diabetic patients with abdominal obesity, through the amelioration of concomitant metabolic abnormalities such as insulin resistance, dyslipidemia, hypertension and inflammation, possible risk factors for the onset of kidney disease. The main aim of the study is therefore to evaluate the renoprotective effect of caloric restriction (CR) on subjects at risk of nephropathy. Secondary aim is to better understand how dietary implementation can modulate renal disease and its associated metabolic abnormalities.

NCT ID: NCT01209403 Completed - Clinical trials for Kidney Failure, Chronic

Insulin-like Growth Factor (IGF-I) in Hemodialysis Patients

Start date: September 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate whether the anabolic potentials of insulin may be used to reverse the catabolic effects of hemodialysis in non-diabetic patients with end-stage renal failure.