Accuracy of Glomerular Filtration Rate (GFR) Estimation Using Creatinine and Cystatin C and Albuminuria
- Conditions
- Chronic Kidney Diseases
- Registration Number
- NCT02433002
- Lead Sponsor
- University of Birmingham
- Brief Summary
The eGFR-C study will assess the accuracy of current and alternative tests of kidney function against a reference test in people with moderate (stage 3) chronic kidney disease (CKD).
- Detailed Description
The eGFR-C study will assess the accuracy of current and alternative tests of kidney function against a reference test in people with moderate (stage 3) CKD. Participants will be recruited from hospital clinics and General Practitioner (GP) practices at six major United Kingdom (UK) centres.
The best measure of kidney function is accepted to be the glomerular filtration rate (GFR), which measures the ability of the kidney to filter blood and is widely used in clinical practice. A low GFR suggests poor kidney function. An estimate of GFR can be obtained from a simple blood test.
Participants will undergo reference GFR testing at study entry with a second follow-up reference test three years later. The reference test involves injecting a small amount of iohexol into a vein and taking blood samples over the next 4 hours to see how quickly the iohexol disappears from the blood stream as a result of glomerular filtration. The rate at which iohexol disappears is equivalent to the level of kidney function. Blood tests for monitoring kidney function, including testing for creatinine and cystatin C, and measurement of urinary albumin will be done every six months during the study period.
Iohexol measured GFR will be accepted as the reference ('gold standard') measure of kidney function against which each GFR-estimating equations will be compared. The alternative estimated measures of GFR, derived from measuring substances (creatinine and cystatin C) in the blood, will be compared against the reference test. An important outcome is how much the reference test changes over the three years of the study, and how well the surrogate measures reflect this change.
The investigators will also collect accurate test cost data for subsequent cost-effectiveness analysis (e.g. do the relative costs of the tests justify any change in practice due to improved performance of one test compared to another?).
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 1249
- Patients with stage 3 CKD (GFR 30-59 mL/min/1.73 m2) as defined internationally, diagnosed using MDRD/CKDEPI eGFR (at least two consecutive test results in this range at least 90 days apart, with the most recent test in the last 12 months)
- Aged 18 years or over
- Written informed consent
- History of untoward reactions to iodinated contrast media or allergy to topical iodine
- Episode of acute kidney injury in previous 6 months (as defined by the Acute Kidney Injury Network criteria)
- Amputation of whole or part-limb
- Pregnant or breastfeeding
- Known current alcohol or drug abuse
- Kidney transplant recipient
- Any condition with an expected survival of less than study duration
- Inability to comply with study schedule and follow-up
- Inability to provide informed consent e.g. due to cognitive impairment
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percentage of estimated Glomerular Filtration Rate values within 30% of 'true' Glomerular Filtration Rate Baseline The accuracy of Glomerular Filtration Rate (GFR) estimating equations is commonly expressed as the P30 value, the percentage of estimated GFR values within 30% of 'true' GFR.
The eGFR-C study will estimate and compare the accuracy and precision of GFR-estimating equations based on the Modification of Diet in Renal Disease (MDRD) equation and three Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equations using either creatinine or cystatin C or a combination of both in people with stage 3 Chronic Kidney Disease (CKD), expressed as the P30 value.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (6)
University Hospital Birmingham NHS Trust (Queen Elizabeth Hospital Birmingham)
🇬🇧Birmingham, West Midlands, United Kingdom
King's College Hospital NHS Foundation Trust
🇬🇧London, Greater London, United Kingdom
East Kent Hospitals NHS Trust (Kent & Canterbury Hospital)
🇬🇧Canterbury, Kent, United Kingdom
University Hospitals of Leicester NHS Trust (Leicester General Hospital)
🇬🇧Leicester, Leicestershire, United Kingdom
Derby Hospitals NHS Foundation Trust (Royal Derby Hospital)
🇬🇧Derby, Derbyshire, United Kingdom
Salford Royal NHS Foundation Trust (Salford Royal Hospital)
🇬🇧Salford, Greater Manchester, United Kingdom