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

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

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00189111
Enrollment
1200
Registered
2005-09-16
Start date
2005-01-31
Completion date
2012-04-30
Last updated
2018-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peripheral Arterial Disease

Keywords

peripheral arterial disease, computed tomography, cardiac asymptomatic, dobutamine magnetic resonance imaging

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.

Interventions

PROCEDURECardiac Imaging + Treatment

Sponsors

Clinical Research Office Imaging Division
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
cardiovascular mortality
cardiovascular morbidity

Secondary

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

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 5, 2026