NCT Number: NCT00189111
Non-invasive Cardiac Screening in High Risk Patients -The GROUND Study
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
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Notify MeKey information
Conditions
Age range
50 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Bronovo Hospital, The Hague, South Holland, Netherlands
About this study
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.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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
Treatment and study plan
Primary outcomes
-
cardiovascular mortality
-
cardiovascular morbidity
Secondary outcomes
-
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
Sponsors and collaborators
Lead sponsor
Clinical Research Office Imaging Division
Other
Registry information
Important dates
- Study start
- 2005
- Study completion
- 2012
- First posted
- Sep 16, 2005
- Registry last updated
- Feb 15, 2018
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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