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Chronic Kidney Disease clinical trials

View clinical trials related to Chronic Kidney Disease.

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NCT ID: NCT02933892 Recruiting - Clinical trials for Chronic Kidney Disease

Benefit of Transradial Approach in Chronic Kidney Disease Population Undergoing Cardiac Catheterization

RADIAL-CKD
Start date: October 2016
Phase: Phase 4
Study type: Interventional

The investigators will conduct a randomized controlled trial that aims to compare the incidence of contrast-induced nephropathy between transradial- and transfemoral-access cardiac catheterization.

NCT ID: NCT02885857 Recruiting - Clinical trials for Chronic Kidney Disease

Safety and Efficacy of Shenyankangfu Tablets for Chronic Kidney Disease

Start date: June 2015
Phase: Phase 4
Study type: Interventional

Safety and efficacy of long-term application of Shenyankangfu Tablets in Large sample of patients with chronic kidney disease.

NCT ID: NCT02844153 Recruiting - Type 2 Diabetes Clinical Trials

Metformin Use in Chronic Kidney Disease: The CKD-Met Study

CKD-Met
Start date: March 2014
Phase: N/A
Study type: Observational

Metformin is the most widely prescribed oral treatment for diabetes, and the only one that showed a survival benefit. Yet, there is no consensus on the optimal dose and withdrawal of metformin in chronic kidney disease (CKD) patients. The aim of the study is to describe the use and side-effects of metformin in CKD patients in routine practice.

NCT ID: NCT02841371 Recruiting - Clinical trials for Chronic Kidney Disease

Early Screening and Diagnosis of CKD

Start date: August 1, 2009
Phase:
Study type: Observational

Chronic kidney disease (CKD) is a global public health problem. The prevalence of CKD in adults in China was 10.8%. Albuminuria measurement and estimating glomerular filtration rate (GFR) are the primary means of screening for CKD in epidemiological investigations. However, there are many important problems to be solved, whether albuminuria test or GFR evaluation. The investigators aim to detect thrice albumin-creatinine ratio (ACR) within three months, with simultaneous test of urinary protein-creatinine ratio (PCR), 24-hour urine protein excretion rate (PER) and 24-hour albumin albumin excretion rate (AER) to compare the effects of different times of screening for CKD and observe the daily physiological variation of ACR, PCR, AER and PER, derive ACR and PCR reference value on the basis of different genders, in order to facilitate the early diagnosis of CKD. Meanwhile, for more accurate assessment of GFR in Chinese populations, the investigators intend to validate beta-trace protein (BTP) based equation to evaluate GFR compared with 99mTc-diethylenetriamine pentaacetic acid (DTPA) renal clearance method. Then to develop GFR estimation equation based on the combination of serum creatinine, cystatin C, β2 -microglobulin and BTP applicable in China.

NCT ID: NCT02829450 Recruiting - Clinical trials for Chronic Kidney Disease

Peritoneal Ultrafiltration to Treat Congestive Heart Failure

Start date: October 2015
Phase: Phase 0
Study type: Observational

The purpose of this study is to determine whether the treatment of peritoneal ultrafiltration can improve survival and quality of life of refractory congestive heart failure with special accent on preserving residual renal function and peritoneal membrane characteristics/

NCT ID: NCT02827253 Recruiting - Clinical trials for Chronic Kidney Disease Requiring Chronic Dialysis

Morphological Changes of the Brain by MRI in Chronic Kidney Disease

KIDBRAIN
Start date: June 2016
Phase: N/A
Study type: Observational

The purpose of this study is to describe brain´s morphological changes induced by chronic kidney disease (CKD) in advanced stages (stages 4 and 5 defined by KDOQI guidelines) and also by haemodialysis using MRI. Based on the hypothesis that hypotension may cause damage in some organs including brain the investigators study if intradialytic hypotension (IDH) causes any type of changes in gray and white matter of the brain.

NCT ID: NCT02813642 Recruiting - Clinical trials for Chronic Kidney Disease

Evaluation of Cardiovascular Risk Factors in Incident Dialysis Patients

Start date: December 8, 2011
Phase: N/A
Study type: Interventional

To evaluate the relationships between bone mineral markers levels at dialysis start and vascular calcification progression during a 2 year follow up

NCT ID: NCT02808572 Recruiting - Clinical trials for Chronic Kidney Disease

New Biomarkers of Bone Mineral Metabolism as Cardiovascular Risk Factors in Chronic Kidney Disease Patients

Start date: March 12, 2013
Phase: N/A
Study type: Interventional

To evaluate the relationships between bone mineral metabolism markers (osteoprotegerin, fibroblast growth factor 23) at inclusion and the occurence of cardiovascular events during a 7 year follow-up.

NCT ID: NCT02616627 Recruiting - Osteoporosis Clinical Trials

Association Between DXA Results and the Complications, Clinical Courses and Outcomes in Chronic Dialysis Patients

Start date: September 2015
Phase:
Study type: Observational

Aims: 1. To determine whether BMD and muscle mass were associated with fractures and other adverse events in dialysis patients. 2. To explore the effects of the interactions among FGF23, calcium, phosphate, PTH and vitamin D on low bone mineral density and sacropenia in dialysis patients. Method: In this study, the investigators plan to use DXA to screen for BMD, relevant novel bone microstructure parameters, and body composition in chronic dialysis patients. Also, the investigators plan to use blood testing to measure the blood level of FGF23, calcium, phosphate, PTH and vitamin D. The investigators conduct a prospectively follow up program for these participants to evaluate clinical courses and outcomes. Patients will receive DXA (including BMD and body composition) tests and blood work at baseline and one-year. Muscle power and physical performance will be measured at baseline, 6 months and one-year.

NCT ID: NCT02578537 Recruiting - Clinical trials for Chronic Kidney Disease

COmparison of the Pharmacodynamics and Pharmacokinetics Ticagrelor Versus Clopidogrel in Patients With CKD and NSTE-ACS

OPT-CKD
Start date: October 2015
Phase: Phase 4
Study type: Interventional

Ticagrelor, a new P2Y12 receptor antagonist, achieve faster, consistent and higher platelet inhibition than clopidogrel, which was considered more noticeable in patients with ACS combining chronic kidney disease(CKD). Nonetheless, the pharmacokinetic properties of ticagrelor in the patients with CKD and NSTE-ACS has not been thoroughly studied. This study was designed to provide PK and PD data of ticagrelor compared with clopidogrel, in order to estimate that ticagrelor is superior to clopidogrel in getting better inhibition of platelet in patients with CKD and NSTE-ACS. P2Y12 inhibitor naïve patients with CKD (eGFR < 60 ml/min/1.73m2 ) and NSTE-ACS will be enrolled in this single-center, prospective, randomized, parallel-control study and randomly assigned in a one-to-one ratio to receive ticagrelor or clopidogrel on top of chronic aspirin treatment. The primary endpoint was the PRU by Verify Now at 30 days after loading dose.