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Renal Insufficiency clinical trials

View clinical trials related to Renal Insufficiency.

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NCT ID: NCT04700631 Completed - Clinical trials for Chronic Renal Failure

Extracellular Vesicles as Biomarkers for Chronic Renal Failure

VE-IRC
Start date: January 1, 2021
Phase: N/A
Study type: Interventional

The recent discovery of extracellular vesicles (EV) as a mechanism of intercellular communication has made it possible to develop a new field of health research and could bring new information on the pathological mechanisms of renal diseases. Definition of physiologic and pathologic values of urinary extracellular vesicles (EVu) between healthy subjects and chronic kidney diseases (CKD) patients could be a new tool for follow up of renal diseases. EV are found in all biological fluids including urine, that's why they are increasingly analyzed in renal pathologies. The main objective of this study is to determine the physiological values and the pathological thresholds of EVu.

NCT ID: NCT04699877 Completed - Clinical trials for Normal Renal Function

A Study to Investigate the Effect of Severe Renal Impairment on Gilteritinib Compared to Healthy Participants With Normal Renal Function

Start date: January 28, 2021
Phase: Phase 1
Study type: Interventional

The purpose of the study was to evaluate the pharmacokinetics of a single oral dose of gilteritinib in male and female participants with severe renal impairment compared to healthy male and female participants with normal renal function. This study also evaluated safety and tolerability of a single oral dose of gilteritinib in male and female participants with severe renal impairment and healthy male and female participants with normal renal function. Part 2 of the study (mild and moderate renal impairment) was not conducted based on the final pharmacokinetic findings from part 1 (severe renal impairment).

NCT ID: NCT04674397 Completed - Renal Failure Clinical Trials

BOne Dysfunction in Donor NEphrectomieS

BONES
Start date: July 29, 2015
Phase:
Study type: Observational

Most dialysis patients die from vascular disease, which is statistically associated with changes related to chronic kidney disease associated mineral bone disorder (CKD-MBD)3-9. Understanding the mechanisms behind this high death rate is crucial to improving the length and quality of life for patients with all grades of kidney disease, including those on dialysis. This is a priority for patients and clinicians alike. Most humans with early CKD are asymptomatic and unaware that they have a problem with their kidneys. Therefore they are unlikely to consult a doctor and early CKD is often unrecognised. Patients who are aware of early CKD often have other co-morbidities including diabetes, hypertension and vascular disease which, in the setting of a clinical study, complicate the identification of changes solely resulting from CKD. However over the past decade living kidney donation has become increasingly common and is now the source of organs for more than 120 patients annually at Manchester's renal transplant centre. Prospective donors are carefully examined and known to have normal kidney function without other co-morbidities. They then undergo a planned unilateral nephrectomy and lose approximately 50% of their kidney mass, creating an immediate state of moderate CKD. Over subsequent months the remaining kidney will hypertrophy and partially correct this, although the mechanisms are unknown. In the immediate post-operative period donors are inpatients on the kidney transplant ward and have regular blood and urine tests meaning that careful study of metabolic processes during their recovery is relatively easy by analysis of serial plasma and urine samples. Sequential changes in the plasma and urine levels of different bone turnover markers and metabolites can be analysed and will provide valuable new information to increase our understanding of the initial stage of CKD-MBD development.

NCT ID: NCT04656795 Completed - Renal Impairment Clinical Trials

PK Study in Subjects With Renal Impairment (Severe and if Required Mild & Moderate) Compared to Subjects With Normal Renal Function

Start date: December 2, 2020
Phase: Phase 1
Study type: Interventional

This is an open-label, non randomised, single-dose, study in male and female subjects with renal impairment (severe and if required mild & moderate) compared to male and female subjects with normal renal function.

NCT ID: NCT04655989 Completed - Clinical trials for Chronic Renal Failure

A Study to Demonstrate the Safety and Effectiveness of the NIKKISO DBB-EXA ES Hemodialysis Delivery System

HEMO
Start date: November 30, 2020
Phase: N/A
Study type: Interventional

The study objective is to verify the safety and effectiveness of the DBB-EXA ES Hemodialysis Delivery System to consistently deliver dialysate of the appropriate quality for infusion.

NCT ID: NCT04646889 Completed - Renal Impairment Clinical Trials

Pharmacokinetic Study of AR882 in Subjects With Various Degrees of Renal Impairment

Start date: January 14, 2021
Phase: Phase 1
Study type: Interventional

This is a 2-segment, multi-center, phase 1, open-label, study evaluating the pharmacokinetics and pharmacodynamics of AR882 in subjects with various degrees of renal impairment.

NCT ID: NCT04641650 Completed - Diabetes Clinical Trials

Pilot Study : FreeStyle Libre Pro Flash Continuous Glucose Monitoring System in Subjects With Diabetes on HemoDIALsis

FSL DIAL
Start date: July 21, 2021
Phase:
Study type: Observational

Continuous monitoring of glucose with a FreeStyle Libre pro sensor in diabetic and dialysis patients

NCT ID: NCT04623710 Completed - Healthy Clinical Trials

Study of ALXN2050 in Participants With Renal Impairment

Start date: July 8, 2021
Phase: Phase 1
Study type: Interventional

This study will investigate the impact of impaired renal function on the plasma pharmacokinetics of ALXN2050 in order to provide dosing recommendations for future indications in individuals with impaired renal function.

NCT ID: NCT04622384 Completed - Acute Kidney Injury Clinical Trials

The Performance of Renal Doppler Ultrasound in Predicting Outcome of Dialysis Weaning

Start date: January 1, 2021
Phase:
Study type: Observational

Acute kidney injury (AKI) is a frequent problem in the intensive care unit (ICU) affecting more than 50 % of patients. AKI is associated with several adverse outcomes, including increased mortality and increased length of ICU- and hospital stay, in particular in patients requiring Renal Replacement Therapy (RRT). Choosing the optimal time for attempting liberation from RRT is still unclear. With this study, we will describe the ability of renal ultrasound in predicting the outcome of dialysis weaning.

NCT ID: NCT04616677 Completed - Renal Impairment Clinical Trials

A Study to Evaluate the Effect of Renal Impairment on JNJ-42847922 in Adult Participants

Start date: March 31, 2021
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the pharmacokinetic of a single oral dose of JNJ-42847922 in adult participants with renal impairment compared with healthy participants with normal renal function.