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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01028703
Other study ID # RKK3922
Secondary ID
Status Completed
Phase N/A
First received December 8, 2009
Last updated December 2, 2015
Start date September 2010
Est. completion date August 2014

Study information

Verified date December 2015
Source University Hospital Birmingham NHS Foundation Trust
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Observational

Clinical Trial Summary

Studies of patients with established kidney disease, even when this is mild, appear to show that they are at high risk of heart failure, stroke and sudden cardiac death. This may be because kidney disease causes stiffening of the arteries in the body which means that the heart and brain are damaged by high blood pressure. By studying patients before and after the removal of a kidney (uni-nephrectomy) for transplantation the investigators will find out for the first time in man the effect of an isolated reduction in kidney function on the structure and function of the arteries and heart.

Hypotheses. An isolated reduction in GFR occuring after surgical uni-nephrectomy is associated with long term adverse cardiac and vascular effects which include:

1. Increased arterial stiffness and left ventricular mass

2. Abnormalities in left ventricular systolic and diastolic function

3. Increased oxidative stress, inflammation and collagen turnover


Recruitment information / eligibility

Status Completed
Enrollment 124
Est. completion date August 2014
Est. primary completion date August 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Potential kidney donor attending University Hospital Birmingham NHS Foundation Trust

Current nationally set Exclusion Criteria:

- Diabetes mellitus

- Atrial fibrillation

- Left ventricular dysfunction (ejection fraction <40% on transthoracic echocardiography)

- History of cardiovascular or pulmonary disease

- Evidence of hypertensive end-organ damage.

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Locations

Country Name City State
United Kingdom University Hospital Birmingham NHS Foundation Trust Birmingham West Midlands

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Birmingham NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Left ventricular mass as measured by CMR and Echocardiography 3 years No
Primary Arterial stiffness as measured by pulse wave velocity 3 years No
Secondary Aortic compliance measured by cardiac magnetic resonance imaging 3 years No
Secondary Left ventricular systolic and diastolic elastance measured by echocardiography; 3 years No
Secondary Oxidative stress, inflammation and collagen turnover measured by blood assays of plasma renin, aldosterone, high sensitivity C-reactive protein (hsCRP), procollagen type III aminoterminal peptide (PIIINP) and C-telopeptide for type I collagen (CITP). 3 years No
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