Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT05508893
Other study ID # 13-693/D
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date November 17, 2014
Est. completion date June 21, 2022

Study information

Verified date August 2022
Source UMC Utrecht
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

SUSPECT is a prospective, single-center, cohort study of 250 military aircrew at the Center for Man in Aviation, Royal Netherlands Air Force. All asymptomatic aircrew (≥40 years) are asked to undergo a coronary CT scan on a voluntary basis, following the exercise electrocardiograms performed at their routine aeromedical examination. Coronary Artery Calcium score (CACS) and CCTA findings are reported.


Recruitment information / eligibility

Status Terminated
Enrollment 250
Est. completion date June 21, 2022
Est. primary completion date June 21, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria: - Military aircrew of the Royal Netherlands Air Force - = 40 years old - Required to undergo cardiac screening (per military aviation regulations) Exclusion Criteria: - Typical angina - Prior myocardial infarction - Prior revascularization therapy (i.e. percutaneous coronary intervention (PCI) and/or coronary artery bypass grafting (CABG)) - Left ventricular ejection fraction <35% - Does not comprehend study requirements, and/or is unwilling or unable to comply to study procedures - CT-related contra-indications - Allergic to iodine contrast. - Renal insufficiency (GFR <60 ml/min/1.73m2, calculated with the Modification of Diet in Renal Disease (MDRD) calculator: http://nephron.org/mdrd_gfr_si. - Severe claustrophobia. - Uncontrolled irregular heart rhythm or tachycardia unresponsive to beta blockade - Pregnancy

Study Design


Intervention

Radiation:
CT Angiography
A CTA will be performed on asymptomatic individuals
Diagnostic Test:
Exercise stress test
A routine exercise stress test will be performed on a bicycle

Locations

Country Name City State
Netherlands Center for Man in Aviation Soesterberg Utrecht
Netherlands Utrecht University Medical Center Utrecht

Sponsors (2)

Lead Sponsor Collaborator
UMC Utrecht Center for Man in Aviation, Royal Netherlands Air Force

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Determine the prevalence and severity of CAD in asymptomatic air crew using CCTA as a primary screening tool 8 Years
Secondary Determine the diagnostic accuracy of clinically relevant CAD of the exercise stress test versus CCTA Both modalities are used to track down clinically relevant CAD. Clinically relevant CAD is defined as a stenosis of >50%. 8 Years
Secondary Compare the incidence of Major Adverse Cardiac Events (MACE) and all-cause mortality in populations screened between primary and secondary screening after 12 months 8 Years
Secondary Compare the incidence of coronary angiograms and revascularization procedures in the population screened with CTA compared to a historical population using CTA as a secondary screening tool 8 Years
Secondary Establish the additive value of coronary artery calcium score (CACS) in addition to clinical risk scores as a predictor of CAD on CCTA 8 Years
See also
  Status Clinical Trial Phase
Recruiting NCT05292079 - CAPTURER PMCF Study ( rEPIC04D )
Recruiting NCT05292092 - Essential Pro PMCF Study ( rEPIC04E )
Recruiting NCT05292118 - Navitian PMCF Study ( rEPIC04C )
Recruiting NCT05292014 - ANGIOLITE PMCF Study ( rEPIC04F )
Completed NCT05292105 - NC Xperience PMCF Study( rEPIC04B)
Completed NCT01435031 - EXPERT CTO: Evaluation of the XIENCE PRIME™ LL and XIENCE Nano™ Everolimus Eluting Coronary Stent Coronary Stents, Performance, and Technique in Chronic Total Occlusions N/A
Terminated NCT01443754 - Hybrid Revascularisation by Combined Coronary Artery Bypass Graft (CABG) and PCI in Multivessel Coronary Disease N/A
Completed NCT00783302 - Study in Subjects Suspected of Having CAD Undergoing VISIPAQUE-enhanced CCTA as Part of Their Routine Medical Care N/A
Completed NCT00543400 - Evaluation of M118 in Percutaneous Coronary Intervention (EMINENCE) Phase 2
Completed NCT05516784 - Impact of CYP2C19 Genotype-guided Clopidogrel and Ticagrelor Treatment on Platelet Function Test and Metabolomics Profile Phase 4
Completed NCT02873052 - MyoVista Measurements in Patients With Atherosclerosis and CAD
Terminated NCT02984891 - Optical Coherence Tomography (OCT) Intravascular Ultrasound (IVUS) Dual Imaging
Completed NCT05292144 - Xperience Pro PMCF Study
Completed NCT02554292 - Post Market Surveillance of SeQuent Please Neo With Scoring Balloon
Active, not recruiting NCT06052319 - A Study to Assess the Engagement and Usefulness of Care4Today Digital Platform for Disease Management in Coronary Artery Disease (CAD) and/or Peripheral Artery Disease (PAD) Population
Completed NCT00265525 - Evaluation of a Web-based Intervention to Promote Physical Activity in Patients With Heart Disease. Phase 3
Completed NCT03570697 - Imaging of Coronary Plaques in Participants Treated With Evolocumab Phase 3
Completed NCT02341664 - Patient and Provider Assessment of Lipid Management Registry
Completed NCT02098772 - Phase III Study Comparing Two Methods of Cardioplegia in Aortic Valve Surgery Custodiol-N Versus Custodiol Phase 3
Recruiting NCT05617599 - SUPRAFLEX CRUZ PMCF Study ( rEpic05 )