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End Stage Renal Disease clinical trials

View clinical trials related to End Stage Renal Disease.

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NCT ID: NCT03318653 Completed - Clinical trials for End Stage Renal Disease

Blood Pressure Measurement in Dialysed Patients

DIALBP
Start date: June 20, 2017
Phase: N/A
Study type: Observational

The objective of the current study is to evaluate the compliance to blood pressure measurements' recommendations in dialysis centers. The idea is to address a questionnaire to physicians, head nurses and patients in order to probe the way to measure blood pressure. The objective is to face the theoretical guideline with what is effectively done.

NCT ID: NCT03315624 Completed - Clinical trials for End Stage Renal Disease

Safety and Clinical Performance of a Dialyzer With a Modified Polysulfone Membrane

eMPORA
Start date: October 6, 2017
Phase: N/A
Study type: Interventional

The clinical investigation will be performed to generate clinical data on clearances and removal rates (for ß2-microglobulin, myoglobin, phosphate, creatinine, and urea) as well as biocompatibility of the modified polysulfone membrane to obtain CE-certification according to the European Medical Device Directive for the FX Coral 600 (TD 16-1) dialyzer.

NCT ID: NCT03311581 Completed - Clinical trials for End Stage Renal Disease

The Feasibility of Propofol TCI in Hemodialysis Patients Undergoing Arteriovenous Shunt Surgery

Start date: September 11, 2017
Phase: Phase 1
Study type: Interventional

Written informed consent must be obtained before any study specific procedures are undertaken. Informed consent will be obtained during pre-operative assessment.

NCT ID: NCT03303144 Completed - Clinical trials for End Stage Renal Disease

Equivalence of Triferic® (Ferric Pyrophosphate Citrate) Administered Via Hemodialysate and Intravenously to Adult CKD-5HD Patients

Start date: October 1, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The main purpose is to establish the equivalence of Triferic iron administered via dialysate into the arterial blood line and into the venous blood line

NCT ID: NCT03301740 Completed - Clinical trials for End Stage Renal Disease

Ultrafiltration Profiling and Outcomes Among Individuals on Maintenance Hemodialysis

Start date: March 12, 2018
Phase: N/A
Study type: Interventional

The rate of fluid removal (ultrafiltration, UF) during hemodialysis (HD) may contribute to cardiovascular morbidity and mortality among individuals receiving maintenance HD. More rapid UF rates are associated with higher morbidity and mortality. Ultrafiltration profiling, the practice of varying UF rates to maximize fluid removal during periods of greatest hydration and plasma oncotic pressures, is one treatment modification that may reduce UF-related harm without necessitating reduction in interdialytic fluid intake or longer HD treatments. To date, UF profiling has not been adequately studied independent of sodium profiling. This study investigates the comparative effect of UF profiling versus non-profiled conventional HD on select cardiovascular and patient-reported outcomes. Participants will complete two phases of UF profiling and two phases of conventional HD and will act as their own controls.

NCT ID: NCT03293589 Completed - Clinical trials for End-stage Renal Disease

Open Versus Endovascular Revascularization in Patients With End-stage Renal Disease

OERESRD
Start date: July 1, 2017
Phase:
Study type: Observational

Treatment of patients with end-stage renal disease and critical limb ischemia still poses challenges to vascular medicine due to limited survival, comorbidities and infrapopliteal involvement of arteriosclerosis in these patients. Most optimal vascular therapy mode has not been finally decided in these patients. Therefore retrospective analysis of patients receiving open surgical and endovascular revascularisation was performed.

NCT ID: NCT03289650 Completed - Clinical trials for End Stage Renal Disease

Extended Release Tacrolimus vs. Twice-Daily Tacrolimus

Start date: September 5, 2017
Phase: Phase 3
Study type: Interventional

The overall aim of the study is to prospectively investigate the impact of two maintenance calcineurin inhibitor immunosuppressive regimens: once-daily extended release tacrolimus and twice-daily tacrolimus on subpopulations of T and B cells and alloreactive T cells as well as on renal allograft function.

NCT ID: NCT03288922 Completed - Hemodialysis Clinical Trials

Protein-bound Toxin Removal Between Limited Blood Flow Super High-flux Online HDF and High-Efficiency Online HDF

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

High-efficiency post-dilution online hemodiafiltration (OL-HDF) using high-flux dialyzer and requiring high blood flow rate (BF ≥400 mL/min) has been reported to enhance protein-bound toxin and middle molecular toxin removal and improve patient survival. Unfortunately, the majority of patients could not reach that high BF because of vascular access issue. This randomized crossover study was conducted to compare these uremic toxin removals between the new modality (limited BF OL-HDF with super high-flux dialyzer) and the control (high-efficiency OL-HDF). The OL-HDF patients were randomized to undergo either new modality or control for 2 weeks before crossover to the other modality for another 2 weeks.

NCT ID: NCT03276390 Completed - ESRD Clinical Trials

A Culturally Targeted Transplant Program

HKTP
Start date: January 18, 2017
Phase: N/A
Study type: Interventional

Hispanic/Latino patients with end-stage renal disease are disproportionately less likely to get a kidney transplant, and specifically, a living donor kidney transplant (LDKT), compared to non-Hispanic whites. Accordingly, without LDKTs, Hispanics experience longer transplant waiting times, shorter patient and graft survival, and worse quality of life. Cultural beliefs and linguistic barriers contribute to the disparity in LDKTs. The objective of the proposed study is to implement and evaluate Northwestern Medicine's® Hispanic Kidney Transplant Program, a culturally-competent transplant center-based intervention, at two transplant centers serving large Hispanic populations. The proposed study will provide valuable knowledge about the potential to rapidly disseminate the HKTP as a novel approach to increase Hispanic LDKTs nationally.

NCT ID: NCT03275077 Completed - Clinical trials for End Stage Renal Disease

To Compare TEG (Thrombelastography) and Conventional Tests in CKD Patients

Start date: March 12, 2016
Phase:
Study type: Observational

Background: Coagulopathy in chronic kidney disease is multifactorial. Both hypocoagulopathy and hypercoaguability are seen. Conventional tests of coagulation (CCTs) end at the formation of thrombin, and do not take into account the interaction of coagulation factors, platelets, RBC etc. By overcoming the above deficiencies, thromboelastography provides a holistic picture of blood coagulation. The present study evaluated the TEG profile of ESRD patients and compared it to CCTs and to controls. Methods: 50 ESRD patients and 50 controls were recruited for the study. Venous samples were withdrawn and platelet count, INR and fibrinogen levels were measured. Simultaneously a Thromboelastography was performed. All samples were drawn prior to initiation of dialysis.