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Renal Insufficiency, Chronic clinical trials

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NCT ID: NCT02496884 Completed - Fibromyalgia Clinical Trials

Safety Study of DS-5565 for Treatment of Fibromyalgia Pain in Subjects With Chronic Kidney Disease

Start date: June 26, 2015
Phase: Phase 3
Study type: Interventional

DS-5565 (mirogabalin) is being studied as treatment for fibromyalgia (FM) pain. Because it is excreted through the kidneys, people who have reduced kidney function will not process the drug as well as with those with normal kidney function, so the dose must be reduced. This study will test two reduced dose levels for both moderately reduced and severely reduced kidney function. The study will test the hypothesis that the drug will be safe and well-tolerated in people who have both fibromyalgia and chronic kidney disease.

NCT ID: NCT02492672 Completed - Clinical trials for Chronic Kidney Disease

Registry to Evaluate Maintenance Treatment With Venofer in Pediatric Patients With Chronic Kidney Disease

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

The current registry is being undertaken to assess the long-term (12 month) safety and tolerability of Venofer in the pediatric population with chronic kidney disease that requires intravenous iron maintenance therapy.

NCT ID: NCT02492620 Completed - Clinical trials for Chronic Kidney Disease

Ferric Citrate for the Transition From CKD Stage 4/5 to CKD Stage 5D

05D
Start date: March 2015
Phase: Phase 3
Study type: Interventional

It is the investigators hypothesis that participants treated with Ferric Citrate (FC) during the non-dialysis CKD stage (4/5) with sufficient duration prior to initiating RRT, will result in improved biochemical control of anemia (Hb, TSAT) and mineral metabolism (P, FGF23) and furthermore, will result in a reduced need for ESA and intravenous iron. The investigators further hypothesize that effective treatment of anemia and mineral metabolism with FC in the pre-dialysis and transition period will result in improved physical functioning, reduced hospitalization and reduced total cost of care when compared to participants receiving contemporaneously provided standard of care therapy.

NCT ID: NCT02488317 Completed - Clinical trials for Chronic Kidney Disease

Empowering Patients On Choices for Renal Replacement Therapy (Aim 3) (EPOCH-RRT)

EPOCH-RRT
Start date: May 2015
Phase: N/A
Study type: Interventional

Empowering Patients On Choices for Renal Replacement Therapy (EPOCH-RRT) study seeks to identify factors that matter the most to patients with kidney disease and study how they are impacted by different types of dialysis. The inclusion of patients, caregivers, and patient advocacy organizations as research partners will assure that the study addresses questions of greatest relevance to patients facing the need for dialysis. For Aim 3, the investigators are going to compare measures related to the decision-making process between patients receiving and not receiving a decision aid focusing on Peritoneal Dialysis and Hemodialysis.

NCT ID: NCT02480751 Completed - Clinical trials for Renal Insufficiency, Chronic

TRK-100STP PhaseII Clinical Study -Chronic Renal Failure (Primary Glomerular Disease/Nephrosclerosis)

Start date: October 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the recommended dose of the sustained-release form of BPS (TRK-100STP low dose or high dose) in Japanese patients with CRF (Primary glomerular disease/nephrosclerosis).

NCT ID: NCT02480699 Completed - Clinical trials for Chronic Kidney Disease

Intra Individual Evaluation of Uremic Toxin Levels in Hemodialysed Patients

EVITUPH
Start date: June 20, 2015
Phase: N/A
Study type: Interventional

Chronic kidney disease (CKD) is characterized by a irreversible decrease of kidney functions. It is characterized by accumulation of solutes called uremic toxins. Uremic toxins levels are implicated in cardiovascular complications associated with CKD. Several protein-bound toxins have been implicated in the increased cardiovascular risk such as indoxyl sulfate (IS), p cresol sulfate (pCS) and more recently the indole acetic acid (IAA). All clinical studies are performed with a single measurement at baseline assuming that the toxin levels are stable over time. The variability of uremic toxins level is not known. Furthermore, little is known concerning determinants of serum toxins level.

NCT ID: NCT02477163 Completed - Clinical trials for Diabetic Nephropathy

Ayurvedic Management of Chronic Kidney Disease

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

The purpose of this study is to determine the effect of multi-dimentional ayurvedic treatment in the patients of various types of chronic kidney disease.

NCT ID: NCT02476526 Completed - Clinical trials for Chronic Kidney Disease

Safety of Low Dose IV Contrast CT Scanning in Chronic Kidney Disease

Start date: September 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to show that the use of low volume iso-osmolar non-ionic radio contrast medium (30 cc) in a thoracic CT Scanning procedure in a selected group of patients with chronic kidney disease (CKD) will avoid contrast induced nephropathy (CIN) in comparison to a similar group of patients with CKD who receive no contrast medium..

NCT ID: NCT02468401 Completed - Clinical trials for Ischemic Heart Disease

Prevention of Contrast Induced Nephropathy in Patients With Advanced Renal Dysfunction Undergoing Coronary Interventions

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

There is a pressing need to find effective strategies for the prevention of contrast induced nephropathy in patients with advanced renal dysfunction. The current study was designed to assess the efficacy of a new protocol for preventing contrast induced nephropathy in patients with advanced renal dysfunction undergoing coronary interventions

NCT ID: NCT02467894 Completed - Hypertension Clinical Trials

Group-based Chronic Kidney Disease Care

Start date: August 2014
Phase: N/A
Study type: Interventional

A two-group randomized clinical trial testing whether group-based care is feasible and will help improve blood pressure control in adult and adolescent patients with chronic kidney disease and hypertension.