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Renal Insufficiency clinical trials

View clinical trials related to Renal Insufficiency.

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NCT ID: NCT02633670 Completed - Renal Failure Clinical Trials

Hemopatch Versus No Hemopatch (Renal Transplant)

Start date: June 2016
Phase: N/A
Study type: Interventional

Kidney transplantation remains one of the most common organ transplanted today but the surgical technique has changed very little from the original pelvic operation. The deceased donor renal transplant poses a particular challenge to the surgeon due to lack of detailed pre operative vascular assessment. The hemopatch is a promising new sealing synthetic hemostatIc agent with a novel dual mechanism of action that is more convenient to apply rather then using other hemostatic agents, which require warming and/or mixing.

NCT ID: NCT02631200 Completed - Clinical trials for Kidney Failure, Chronic

Advance Care Planning With Older Patients Who Have End-stage Kidney Disease

ACREDiT
Start date: December 2016
Phase: N/A
Study type: Interventional

This study will test the feasibility of carrying out a randomised controlled trial, incorporating a mixed methods process evaluation, to evaluate advance care planning with older patients who have end-stage kidney disease.

NCT ID: NCT02629224 Completed - Clinical trials for Patients With Impaired Renal Function and Haemodialysis

ASP8825 - Pharmacokinetics Study in Patients With Impaired Renal Function and Haemodialysis

Start date: February 2008
Phase: Phase 1
Study type: Interventional

The objective of this study is to evaluate the pharmacokinetics and safety of ASP8825 in patients with impaired renal function and haemodialysis.

NCT ID: NCT02627066 Completed - Renal Failure Clinical Trials

Optimizing Cardiovascular Health and Physical Function in Hemodialysis Patients Through Volume Control and Exercise

VCE
Start date: December 2015
Phase: N/A
Study type: Interventional

This is a 12 month randomized clinical trial in which patients with renal failure undergoing maintenance hemodialysis (MHD) therapy will be placed on a volume reduction protocol that includes a novel low sodium dietary education program mediated by a lifestyle interventionist with significant collaboration from the existing clinic staff. Participating patients will be randomized to receive: 1) the volume control protocol alone (VC), or 2) the volume control protocol + physical activity and exercise counseling (VCE) from the lifestyle interventionist (LI). A research dietitian (RD), working in collaboration with the existing clinic RD, will develop a program to immerse clinics in a culture of sodium restriction. The research RD will train the LI and other clinic staff (nurses, technicians, etc) to help disseminate this program, modeled after the clinic-wide dissemination approach used in Izmir, Turkey (Dr. Ercan Ok). In addition, the LI will provide exercise and physical activity counseling to the participants randomized to the exercise group, utilizing a SCT-based approach. The Investigators hypothesize that mean arterial pressure will be reduced, and physical function increased, in all patients at 12 months, but the magnitude of these improvements will be greater in the VCE group.

NCT ID: NCT02626676 Completed - Clinical trials for Renal Insufficiency, Chronic

Educational Programme Impact on Serum Phosphate Control

EPIC
Start date: November 2015
Phase: N/A
Study type: Interventional

Background: In Chronic Kidney Disease patients, it is crucial to begin treatment as soon as possible in order to minimize the complication-related risks. Encouraging patients to adhere to their treatment plans is a great challenge for health care professionals. Objectives: The aim of this study is to evaluate the impact of a nutrition educational programme on the hyperphosphatemia using the transtheoretical model of eating behavior. Subjects and Methods: A prospective Interventional study is being conducted in a dialysis centre with 180 stage 5D Chronic Kidney Disease patients who exhibit phosphate serum levels > 5.5 mg/dL. The educational intervention consists of lectures and group dynamics sessions performed during dialysis sessions. Anthropometric, clinical, demographic and laboratory parameters (serum phosphorus concentration will be evaluated and the transtheoretical model of eating behavior (TMFB) will be applied pre- and post-intervention.

NCT ID: NCT02621918 Completed - Clinical trials for End Stage Renal Failure on Dialysis

The Effects of Exercise in End-stage Renal Disease Patients Undergoing Hemodialysis

EESRDS
Start date: March 2013
Phase: N/A
Study type: Interventional

We aimed to investigate the effect of a progressive resistance training and aerobic training protocol on functional capacity, body composition and quality of life.

NCT ID: NCT02621762 Completed - Clinical trials for End Stage Renal Failure on Dialysis

Pilot Study to Investigate the Effects of Increased Dialysate Magnesium and Dialysate Bicarbonate on the Calcification Propensity of Serum

BicMag
Start date: December 2015
Phase: N/A
Study type: Interventional

The study aims to determine the effect size of magnesium and bicarbonate supplementation as a basis for future randomized controlled trials aiming at the T50-guided improvement of hard clinical endpoints in dialysis patients.

NCT ID: NCT02621112 Completed - Renal Failure Clinical Trials

HBV Vaccine in Renal Failure Patients

Start date: January 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Hepatitis B virus infection remains an important clinical issue among patients on renal replacement therapy. Seroconversion rate as defined by an anti-HBs Ab titer > 10 IU/L after intramuscular hepatitis B vaccination (HBVv) remains poor in this cohort. Factors associated with inadequate anti-HBs response include older age, diabetes mellitus, obesity and low hepatitis B vaccine dose. Various small-scale studies including multiple high dose intramuscular vaccination or multiple small dose intradermal vaccination were attempted with variable response. Recent study on dose sparing seasonal influenza vaccine delivered via a novel intradermal microneedle has demonstrated good immunogenic responses similar to full-dose intramuscular vaccination. Imiquimod, a synthetic TLR7 agonist useful for the treatment of DNA virus infection, has been shown to improve vaccine immunogenicity. The investigators therefore propose a prospective, randomized study to compare the safety and immunogenicity of intradermal hepatitis B vaccination with this novel device with intramuscular in patients on renal replacement therapy.

NCT ID: NCT02607280 Completed - Clinical trials for Diabetic Peripheral Neuropathic Pain

DS-5565 Phase III Study for Renal Impairment in Japanese Subjects

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

Investigate the safety and efficacy of DS-5565 in Japanese subjects with Diabetic Peripheral Neuropathic Pain (DPNP) with renal impairment or Post-Herpetic Neuralgia (PHN) with renal impairment.

NCT ID: NCT02607111 Completed - Kidney Failure Clinical Trials

A New Anticoagulation Method Using Dalteparin in Quotidian and Nocturnal Home Hemodialysis Patients

Start date: August 2016
Phase: Phase 4
Study type: Interventional

This study evaluates the optimal dosage and safety of Dalteparin when used as an anticoagulant for hemodialysis therapies.