End-Stage Renal Disease Clinical Trial
Official title:
Arterial Stiffness in Healthy Subjects and Patients With End‐Stage‐ Renal Disease: A Feasibility Study
Verified date | March 2016 |
Source | Ottawa Hospital Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Ethics Review Committee |
Study type | Observational |
People with kidney failure have a higher chance of getting disease in the blood vessels and this result in a decreased elasticity of the arteries of their body which make them very stiff or hard. It appears that stiffer arteries with a decreased elasticity increase the risk of stroke and heart disease. A novel way to know the stiffness of blood vessels is by a method called "applanation tonometry", which measures the "pulse wave velocity" of major blood vessels such as the aorta, carotid and femoral arteries. The purpose of our study is to determine if we can measure arterial stiffness reliably and accurately using this method in healthy people and in people with kidney failure receiving hemodialysis treatments at our centre. Also, we would like to know how stiff these arteries in healthy people are. If we demonstrate that the method is reliable and accurate in these 2 groups of participants at our centre, a future larger study is planned to determine if we can use measures of arterial stiffness to evaluate the risk of stroke and heart disease in people with kidney failure receiving hemodialysis. The research study will take place at the Ottawa Hospital-Riverside Campus.
Status | Terminated |
Enrollment | 36 |
Est. completion date | March 2016 |
Est. primary completion date | March 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
HEALTHY SUBJECT GROUP Inclusion criteria: - Age: >18 years - Able to provide informed consent Exclusion criteria - History of cardiovascular disease and/or hypertension (blood pressure >140/90 mm Hg) - History of diabetes mellitus - History of liver or kidney disease, cancer and/or any lymphoproliferative disease - Currently receiving medication for any medical condition or illness - Body Mass Index (BMI) = 30 Kg/m2 - Pregnancy - Any condition that limits functional ability and precludes participation - Current smoker (>15 cigarettes per day) in the last 6 months. - Former smoker (> 20 cigarettes per day) who stopped smoking < 2 years ago. - Excessive alcohol intake (men >14 drinks per week; women: > 9 drinks per week). - Psychoactive or performance-enhancing drug abuse. END-STAGE RENAL DISEASE (ESRD) GROUP Inclusion Criteria: - Adult patient (age: >18 years) with ESRD (estimated glomerular filtration rate: <15 ml/min/m2) - Receiving hemodialysis treatments, with no expected renal recovery - Having received regular in-Centre Hemodialysis at TOH for at least the past 3 weeks - Able to provide informed consent. Exclusion Criteria: - Atrial fibrillation (as it frequently results in transient or persistent rapid heart rates and these changes overestimate aortic stiffness). - Active cancer or history of cancer in the past 5 years. - Pregnancy - Any condition that limit the patient's ambulatory ability and preclude participation on this basis - Mechanical, bioprosthetic heart valves or mechanical assisting devices (these conditions may change myocardial stiffness and the volumetric properties of the left ventricle leading to diastolic dysfunction and these physiologic changes may modify the waveforms of the cf- APWV). - Pre-dialysis systolic blood pressure = 200 mm Hg recorded in the last 6 dialysis treatments (2 weeks). - Inability to measure blood pressure in at least one arm. - Current smoker (>15 cigarettes per day) in the last 6 months [Daily cigarette consumption (>15 cigarettes per day) adjusted by age, education level and other confounders has been found to be independently associated with the risk of hypertension]. |
Observational Model: Case Control, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Canada | The Ottawa Hospital - Riverside campus | Ottawa | Ontario |
Lead Sponsor | Collaborator |
---|---|
Ottawa Hospital Research Institute | The Ottawa Hospital, University of Ottawa |
Canada,
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Normative Pulse Wave Velocity Values | We will calculate the mean, standard deviation and 95% confidence interval of the pulse wave velocity values and Augmentation index in our defined populations. | 11 months | No |
Primary | Reliability of carotid-femoral Pulse Wave Velocity measurements | We will estimate the Pulse Wave Velocity differences and the intra-class correlation coefficient (ICC) between the 2 examinations (test-retest) recorded in the same subject 1 week apart. We will also estimate the examiner's reliability by the inter-rater agreement through the ICC and limits of agreement. | 1 week | No |
Secondary | Accuracy of the carotid-femoral Pulse Wave Velocity measurements | This will be estimated by calculating the mean, standard deviation and 95% confidence interval of the Pulse Wave Velocity differences between our healthy group and the age-adjusted mean values from a historical healthy control group | 1 week | No |
Secondary | Subject satisfaction and procedure discomfort | This will be accomplished by surveying subjects at the end of the testing procedure using a Likert-type questionnaire | 1 week | No |
Secondary | Recruitment Efficacy | We will assess the proportion of patients with End-Stage Renal disease (ESRD) who consented to the testing procedure relative to the number of eligible and screened participants | 11 months | No |
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