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Non-invasive Cardiac Screening in High Risk Patients -The GROUND Study

Primary Purpose

Peripheral Arterial Disease

Status
Completed
Phase
Phase 3
Locations
Netherlands
Study Type
Interventional
Intervention
Cardiac Imaging + Treatment
Sponsored by
Clinical Research Office Imaging Division
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Peripheral Arterial Disease focused on measuring peripheral arterial disease, computed tomography, cardiac asymptomatic, dobutamine magnetic resonance imaging

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients with peripheral arterial disease, diagnosed by the vascular surgeon Patients must provide consent in writing after proper education and discussion with the treating physician and/or research physician Patients must be aged 50 years or over Exclusion Criteria: History of symptomatic cardiac disease Cardiac rhythm other than sinus Unable to sustain a breath-hold for 25 seconds Asthma (contraindication beta-blockers) Contra-indications to MRI examination. Contra-indications to iodine contrast. Severe arterial hypertension (>220/120 mmHg) Significant aortic stenosis Unable to remain in supine position for at least 60 minutes Morbidly obese (BMI > 40) Renal insufficiency (creatinine >140mmol/l) Severe physical deterioration due to concomitant illness Language barrier Acute coronary syndrome Contra-indications to dobutamine

Sites / Locations

  • Meander Medical Center
  • St. Antonius Hospital
  • Bronovo Hospital
  • University Medical Center Groningen
  • University Medical Center Utrecht

Outcomes

Primary Outcome Measures

cardiovascular mortality
cardiovascular morbidity

Secondary Outcome Measures

Fatal and non-fatal myocardial infarction
Fatal and non-fatal stroke
Vascular interventions
Amputation
Aortic rupture
End stage renal failure
Extra cranial hemorrhage
Complications of CABG or PTCA
All cause mortality

Full Information

First Posted
September 12, 2005
Last Updated
February 14, 2018
Sponsor
Clinical Research Office Imaging Division
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1. Study Identification

Unique Protocol Identification Number
NCT00189111
Brief Title
Non-invasive Cardiac Screening in High Risk Patients -The GROUND Study
Official Title
Non-invasive Cardiac Screening in High Risk Patients -The GROUND Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Clinical Research Office Imaging Division

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to find out if subjecting cardiac high risk patients to non invasive cardiac imaging, followed by treatment will improve survival and quality of life
Detailed Description
Peripheral arterial disease (PAD) is a common disease associated with a considerably increased risk of future events and with a high prevalence of coronary artery disease (CAD). Improvement of the prognosis of this patient group is needed. Screening for CAD has become an option with recent developments in CT-angiography and MR stress testing. It is unknown if high-risk patient groups benefit from screening through non-invasive cardiac imaging. Therefore we propose to study whether a cardiac imaging algorithm, using non-invasive imaging techniques followed by evidence-based treatment will reduce the risk of cardiovascular disease in cardiac asymptomatic PAD patients. The GROUND study is designed as a prospective, multi-center, randomized clinical trial. Patients with peripheral arterial disease, but yet without a history of symptomatic cardiac disease will be asked to participate. All patients receive a proper therapeutic advice before randomization. Half of the recruited patients will enter the 'control group' and only receive CT calcium scoring. The other half of the recruited patients (index group) will undergo the non invasive cardiac imaging algorithm followed by evidence-based treatment. First patients undergo CT calcium scoring and CT angiography. Patients with a left main (or equivalent) coronary artery stenosis on CT angiography will be referred to a cardiologist without further imaging. All other patients in this group will undergo Dobutamine Stress Magnetic Resonance (DSMR) testing. Patients with a DSMR positive for ischemia will also be referred to a cardiologist. Most referred patients will very likely undergo conventional coronary artery angiography and cardiac interventions (CABG or PCI) if indicated. All participants of the trial will enter a 5 year follow up period for the occurrence of future cardiovascular events. Interim analysis will take place and based on power calculations about 1200 patients are needed to reach significance. Implications The GROUND study will provide new insight into the question whether non-invasive cardiac imaging reduces the risk of cardiovascular events in patients with peripheral arterial disease, but yet without symptoms of coronary artery disease as an example of a high risk patient group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease
Keywords
peripheral arterial disease, computed tomography, cardiac asymptomatic, dobutamine magnetic resonance imaging

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1200 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Cardiac Imaging + Treatment
Primary Outcome Measure Information:
Title
cardiovascular mortality
Title
cardiovascular morbidity
Secondary Outcome Measure Information:
Title
Fatal and non-fatal myocardial infarction
Title
Fatal and non-fatal stroke
Title
Vascular interventions
Title
Amputation
Title
Aortic rupture
Title
End stage renal failure
Title
Extra cranial hemorrhage
Title
Complications of CABG or PTCA
Title
All cause mortality

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with peripheral arterial disease, diagnosed by the vascular surgeon Patients must provide consent in writing after proper education and discussion with the treating physician and/or research physician Patients must be aged 50 years or over Exclusion Criteria: History of symptomatic cardiac disease Cardiac rhythm other than sinus Unable to sustain a breath-hold for 25 seconds Asthma (contraindication beta-blockers) Contra-indications to MRI examination. Contra-indications to iodine contrast. Severe arterial hypertension (>220/120 mmHg) Significant aortic stenosis Unable to remain in supine position for at least 60 minutes Morbidly obese (BMI > 40) Renal insufficiency (creatinine >140mmol/l) Severe physical deterioration due to concomitant illness Language barrier Acute coronary syndrome Contra-indications to dobutamine
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
W. Mali, PhD
Organizational Affiliation
UMC Utrecht
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
M. Oudkerk, PhD
Organizational Affiliation
University Medical Center Groningen
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
M.L. Bots, PhD
Organizational Affiliation
Julius Center, University Medical Center Utrecht
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
F. Zijlstra, PhD
Organizational Affiliation
University Medical Center Groningen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Meander Medical Center
City
Amersfoort
State/Province
Utrecht
ZIP/Postal Code
3800 BM
Country
Netherlands
Facility Name
St. Antonius Hospital
City
Nieuwegein
State/Province
Utrecht
ZIP/Postal Code
3435 CM
Country
Netherlands
Facility Name
Bronovo Hospital
City
The Hague
State/Province
Zuid-Holland
ZIP/Postal Code
2597 AX
Country
Netherlands
Facility Name
University Medical Center Groningen
City
Groningen
ZIP/Postal Code
9700 RB
Country
Netherlands
Facility Name
University Medical Center Utrecht
City
Utrecht
ZIP/Postal Code
3584CX
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
18673542
Citation
de Vos AM, Rutten A, van de Zaag-Loonen HJ, Bots ML, Dikkers R, Buiskool RA, Mali WP, Lubbers DD, Mosterd A, Prokop M, Rensing BJ, Cramer MJ, van Es HW, Moll FL, van de Pavoordt ED, Doevendans PA, Velthuis BK, Mackaay AJ, Zijlstra F, Oudkerk M. Non-invasive cardiac assessment in high risk patients (The GROUND study): rationale, objectives and design of a multi-center randomized controlled clinical trial. Trials. 2008 Aug 1;9:49. doi: 10.1186/1745-6215-9-49.
Results Reference
derived

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Non-invasive Cardiac Screening in High Risk Patients -The GROUND Study

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