Myocardial Microvascular Disease in ESRD (MICROCARD)
Primary Purpose
End Stage Renal Disease, Myocardial Microvascular Disease
Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Invasive FFR + CFR measurements are performed during coronary angiography using a pressure guide wire
Sponsored by
About this trial
This is an interventional prevention trial for End Stage Renal Disease focused on measuring End stage renal disease, myocardial microvascular disease, cardiorenal syndrome, coronary flow reserve, index of microvascular resistance, Patients with end stage renal disease scheduled or not for kidney or kidney + pancreatic transplantation
Eligibility Criteria
Inclusion Criteria:
- Patients age > 18 years with end stage renal disease under dialysis and/or scheduled for kidney or kidney + pancreatic transplantation
- Having a non invasive detection of myocardial ischemia and agreeing to participate (signed informed consent document)
Exclusion Criteria:
Past medical history of
- Acute coronary syndrome
- Hypertrophic cardiomyopathy
- severe aortic and/or mitral valvular disease (grade ≥ 3)
- Known contraindications to adenosine injection: AV block grade ≥ 2 and/or sinoatrial block unless prior implantation of a pace maker, asthma, allergic reaction to adenosine.
Sites / Locations
- Service de Cardiologie D - Hôpital Louis Pradel - Hospices Civils de Lyon
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Experimental
Arm Label
comparator
coronary angiography group
Arm Description
One group of patients with no myocardial ischemia on non invasive testing will be followed up for 2 years
One group of patients with myocardial ischemia on non invasive testing will undergo coronary angiography and measure of FFR + CFR to detect myocardial microvascular disease
Outcomes
Primary Outcome Measures
Major cardiovascular events
Major cardiovascular events
Death (all cause)
Acute coronary syndromes (STEMI, NSTEMI, UA)
New onset of stable angina
New onset of congestive heart failure or progression of previously known congestive heart failure (need for therapeutic intensification and/or hospital admission)
Cardiogenic shock
Stroke
Severe cardiac arrhythmia (FV, VT)
New onset of atrial fibrillation
Secondary Outcome Measures
Incidence of myocardial microvascular disease detected by FFR + CFR in ESRD patients with myocardial ischemia on non invasive tests.
Full Information
NCT ID
NCT01291771
First Posted
February 7, 2011
Last Updated
January 15, 2015
Sponsor
Hospices Civils de Lyon
1. Study Identification
Unique Protocol Identification Number
NCT01291771
Brief Title
Myocardial Microvascular Disease in ESRD
Acronym
MICROCARD
Official Title
Detection and Outcomes of Myocardial Microvascular Disease in Patients With End Stage Renal Disease
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Terminated
Study Start Date
January 2011 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
January 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospices Civils de Lyon
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Cardiovascular diseases are the leading cause of mortality in patients with end stage renal disease (ESRD). They often have myocardial ischemia (a major predictor of mortality) on non invasive testing (Stress echocardiography and/or myocardial perfusion scintigraphy) but the incidence of significant coronary stenosis (>70%) is low. The goal of this observational study is to evaluate the incidence and clinical outcomes of proven myocardial microvascular disease in patients with end stage renal disease scheduled or not for kidney transplantation. These patients routinely undergo non invasive detection of myocardial ischemia. Patient included in the study will be followed up for 2 years for major cardiovascular events. Patients with detected myocardial ischemia during non invasive testing are being explored by coronary angiography. During coronary angiography additional detection of myocardial microvascular disease is being performed by simultaneous measurement of Fractional Flow Reserve (FFR) and Coronary Flow Reserve (CFR) followed by calculation of the index of microcirculatory resistance (IMR).
Comparison of cardiovascular outcomes between patients with and without myocardial ischemia and patients with and without myocardial microvascular disease will be performed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End Stage Renal Disease, Myocardial Microvascular Disease
Keywords
End stage renal disease, myocardial microvascular disease, cardiorenal syndrome, coronary flow reserve, index of microvascular resistance, Patients with end stage renal disease scheduled or not for kidney or kidney + pancreatic transplantation
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
comparator
Arm Type
Other
Arm Description
One group of patients with no myocardial ischemia on non invasive testing will be followed up for 2 years
Arm Title
coronary angiography group
Arm Type
Experimental
Arm Description
One group of patients with myocardial ischemia on non invasive testing will undergo coronary angiography and measure of FFR + CFR to detect myocardial microvascular disease
Intervention Type
Procedure
Intervention Name(s)
Invasive FFR + CFR measurements are performed during coronary angiography using a pressure guide wire
Intervention Description
The guide is placed in the distal segment of the coronary artery to measure instantaneously distal pressure and temperature with a tip sensor. Proximal pressure and temperature are being measured from the probe used to catheterize the coronary vessel and from the shaft of the guide. After basal measurement, intracoronary injection of 150µg of adenosine is performed to induce peripheral vasodilatation leading to hyperaemia in the vessel. Additional injection of 3mL 0.9% saline bolus at room temperature at the time of hyperaemia is performed to calculate CFR from transit mean time. FFR and CFR are being recorded at the time of hyperaemia. Subsequently IMR is being calculated from distal pressure and transit mean time. The measurements will be performed in the LAD, circumflex and right coronary arteries.
Primary Outcome Measure Information:
Title
Major cardiovascular events
Description
Major cardiovascular events
Death (all cause)
Acute coronary syndromes (STEMI, NSTEMI, UA)
New onset of stable angina
New onset of congestive heart failure or progression of previously known congestive heart failure (need for therapeutic intensification and/or hospital admission)
Cardiogenic shock
Stroke
Severe cardiac arrhythmia (FV, VT)
New onset of atrial fibrillation
Time Frame
Inclusion: 1 year - Follow up: 2 years
Secondary Outcome Measure Information:
Title
Incidence of myocardial microvascular disease detected by FFR + CFR in ESRD patients with myocardial ischemia on non invasive tests.
Time Frame
Inclusion: 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients age > 18 years with end stage renal disease under dialysis and/or scheduled for kidney or kidney + pancreatic transplantation
Having a non invasive detection of myocardial ischemia and agreeing to participate (signed informed consent document)
Exclusion Criteria:
Past medical history of
Acute coronary syndrome
Hypertrophic cardiomyopathy
severe aortic and/or mitral valvular disease (grade ≥ 3)
Known contraindications to adenosine injection: AV block grade ≥ 2 and/or sinoatrial block unless prior implantation of a pace maker, asthma, allergic reaction to adenosine.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Denis ANGOULVANT, Dr
Organizational Affiliation
Hospices Civils de Lyon
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service de Cardiologie D - Hôpital Louis Pradel - Hospices Civils de Lyon
City
Bron
ZIP/Postal Code
69677
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
22344775
Citation
Bejan-Angoulvant T, Bergerot C, Juillard L, Mezergues A, Morelon E, Pouteil-Noble C, Andre-Fouet X, Angoulvant D. Myocardial microvascular disease and major adverse cardiovascular events in patients with end-stage renal disease: rationale and design of the MICROCARD study. Nephrol Dial Transplant. 2012 Jul;27(7):2886-91. doi: 10.1093/ndt/gfs008. Epub 2012 Feb 17.
Results Reference
derived
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Myocardial Microvascular Disease in ESRD
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