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Renal Insufficiency, Chronic clinical trials

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NCT ID: NCT03459807 Completed - Blood Pressure Clinical Trials

Blood Pressure Lowering in Dialysis (BOLD) Trial

BOLD
Start date: March 23, 2018
Phase: Phase 2
Study type: Interventional

Blood pressure may be one of the most important modifiable risk factors for cardiovascular disease in patients with end-stage-renal-disease undergoing maintenance hemodialysis. Although a systolic blood pressure <140 mmHg treatment target has been recommended, there remains uncertainty on which blood pressure should be targeted, more specifically that measured in the dialysis unit or at home. Observational studies have reported a paradoxical U-shaped associated with dialysis unit (pre-dialysis) systolic blood pressure and cardiovascular events and death (where blood pressure below 140 mmHg is actually linked with poor outcomes). Conversely, the same studies have reported a linear association between higher home systolic blood pressure and worse clinical outcomes, where blood pressure below 140 mmHg is associated with better outcomes. This pilot clinical trial aims to address this important question.

NCT ID: NCT03458338 Completed - Hypertension Clinical Trials

Prevalence of Chronic Kidney Disease (CKD) and Risk Factors in Sub-Saharan Africa

RenalOne
Start date: December 8, 2010
Phase: N/A
Study type: Observational

Prospective cross-sectional study at the outpatient clinic (OPC) of the Bagamoyo District Hospital (BDH) in Tanzania. Assessment of basic epidemiological data (Point prevalence and risk factors) on CKD with simple clinical, laboratory tests and the patients history. After informed consent blood samples are taken for complete blood count, serum creatinine, HbA1c, HIV-Screening, and urine samples for dipstick, urine sediment, and albumin-creatinine ratio. Further, office blood pressure, weight and height are taken. Further, patients history are asked by a questionnaire (i.e.history of infectious and cardiovascular diseases and basic demographic data: i.e. sex, age). CKD is defined as the presence of either impaired kidney function and/or albuminuria based on a one-time measurement. Primary outcome of the study are prevalence rates of CKD and the impact of non-communicable and communicable disorders on CKD.

NCT ID: NCT03454022 Completed - Clinical trials for Kidney Failure, Chronic

Decision-Aid for Renal Therapy Pilot Trial

Start date: March 16, 2017
Phase: N/A
Study type: Interventional

Successful communication between patients, caregivers, and physicians can improve how patients feel about their treatment. Our recent studies of older dialysis patients find, however, that many patients do not engage in this type of communication about treatment options. This study aims to determine whether the Decision-Aid for Renal Therapy (DART), a web-based program, can improve shared decision-making (decisions where patients are actively engaged) among patients, caregivers, and physicians, and improve certainty and satisfaction in treatment decisions.

NCT ID: NCT03451019 Completed - Clinical trials for Chronic Kidney Disease

Different Effects of Non-calcium Phosphate Binders on Serum Calcium

Start date: March 1, 2018
Phase: Phase 4
Study type: Interventional

Sevelamer hydrochloride (SE) can increase intestinal calcium absorption in contrast to lanthanum carbonate (LA). Study compared effect of LA and SE on serum and urine phosphate and calcium, and hormones regulating mineral-bone metabolism.

NCT ID: NCT03446794 Completed - Clinical trials for Cardiovascular Diseases

Left Atrial Appendage Occlusion With WATCHMAN® Device in Patients With Non-valvular Atrial Fibrillation and End-stage Chronic Kidney Disease on Hemodialysis

WATCH-HD
Start date: March 14, 2018
Phase:
Study type: Observational [Patient Registry]

Atrial fibrillation (AF) is more common in patients with renal disease compared to the general population an risk increase to as much as 10 times in patients on hemodialysis (HD). Stroke is an important cause of morbidity, mortality and suffering for patients with end-stage chronic kidney disease (ESCKD) on hemodialysis.The risk of bleeding in these patients can be roughly 5-fold higher that without it. Current guidelines recommend the use of oral anticoagulants (AO) to prevent stroke or systemic thromboembolism in high-risk patients with AF. Left atrial appendage occlusion (LAAO) reduces the risk of bleeding while allows thromboembolic stroke prevention. The aim of the study is to assess the procedural safety on stroke and bleeding prevention of LAAC in patients with non-valvular atrial fibrillation (NVAF) and ESCKD on HD.

NCT ID: NCT03439137 Completed - Clinical trials for Anemia; Hemodialysis Dependent Chronic Kidney Disease

Efficacy and Safety Study to Evaluate MT-6548 in Hemodialysis Subjects Currently Receiving ESAs With Anemia Associated With Chronic Kidney Disease in Japan

Start date: February 14, 2018
Phase: Phase 3
Study type: Interventional

For hemodialysis subjects currently receiving ESAs with anemia associated with chronic kidney disease, demonstrate non-inferiority of MT-6548 compared to darbepoetin alfa using Hb value and evaluate long-term safety of MT-6548.

NCT ID: NCT03434145 Completed - Clinical trials for Chronic Kidney Diseases

Changes of Ocular Structures After Hemodialysis in Patients With Chronic Kidney Diseases

Start date: September 9, 2016
Phase: N/A
Study type: Observational

To evaluate the effect of hemodialysis on various ophthalmologic parameters in patients with end-stage kidney disease (ESRD).

NCT ID: NCT03431623 Completed - Clinical trials for Anemia of Chronic Kidney Disease

CKD-11101 Phase 3 SC Study

Start date: May 2015
Phase: Phase 3
Study type: Interventional

The aim of this study was to compare and evaluate efficacy and safety of subcutaneous CKD-11101 versus Darbepoetin alfa in patients who have renal anemia not on dialysis.

NCT ID: NCT03428594 Completed - Clinical trials for Anemia of Chronic Kidney Disease

CKD-11101 Phase 3 IV Study in Patients Who Had Renal Anemia Receiving Hemodialysis

Start date: June 2015
Phase: Phase 3
Study type: Interventional

The aim of this study was to compare and evaluate efficacy and safety of intravenous CKD-11101 versus Darbepoetin alfa in patients who have renal anemia receiving hemodialysis.

NCT ID: NCT03427801 Completed - Clinical trials for Anemia of Chronic Kidney Disease

Effect of Erythropoiesis-Stimulating Agent Therapy in Patients Receiving Palliative Care of Chronic Kidney Disease

Start date: March 1, 2017
Phase:
Study type: Observational

An observational study to evaluate the effect of erythropoiesis-stimulating agents in treating anaemia of renal disease among adult patients receive palliative care instead of dialysis.