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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03659526
Other study ID # IRAS Project ID 136434
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 21, 2016
Est. completion date October 31, 2021

Study information

Verified date September 2018
Source University Hospital of Wales
Contact Imran D Sunderji
Phone +441482 875875
Email imran.sunderji@nhs.net
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients with chest pain on exertion need a reliable non-invasive test to identify if they have inducible myocardial ischaemia. This would reduce the use of diagnostic coronary arteriography, avoid its risks and costs, and guide clinical decisions. Conventional stress echocardiography has poor reproducibility because it relies on qualitative and subjective interpretation. Quantitative approaches based on precise and reliable measurements of myocardial velocity, strain, strain rate and global longitudinal strain have been shown to be able to accurately diagnose myocardial ischaemia. A more accurate test using myocardial velocity imaging was not implemented by ultrasound vendors although it provided an objective measurement of myocardial functional reserve on a continuous scale from normality to severe ischaemia.

The investigators propose an original approach to create a diagnostic software tool that can be used in routine clinical practice. The investigators will extract and compare quantitative data obtained through myocardial velocity imaging and speckle tracking in subjects who undergo dobutamine stress echocardiography.

The data will be analysed using advanced computational mathematics including multiple kernel learning and joint statistics applied to multivariate data across multiple dimensions (including velocity, strain and strain rate traces). This approach will be validated against quantitative coronary arteriography and fractional flow reserve. The results will be displayed as parametric images and placed into a reporting tool. The output will determine the presence and severity of myocardial ischaemia. These new tools will have the capacity for iterative learning so that the precision of the diagnostic conclusions can be continuously refined.


Recruitment information / eligibility

Status Recruiting
Enrollment 390
Est. completion date October 31, 2021
Est. primary completion date October 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 89 Years
Eligibility Inclusion Criteria:

- Chest pain, chest pain equivalent

Exclusion Criteria:

- acute coronary syndrome with elevated troponin, severe heart valve disease, uncontrolled hypertension (resting SBP >200mmHg), cardiomyopathy, contraindication to dobutamine, pregnancy

Study Design


Intervention

Diagnostic Test:
Deformation imaging
Deformation parameters derived using myocardial velocity imaging or speckle tracking

Locations

Country Name City State
Belgium UZ Leuven Leuven
Sweden Danderyd Hospital Stockholm
United Kingdom University Hospital Wales Cardiff
United Kingdom Castle Hill Hospital Cottingham

Sponsors (5)

Lead Sponsor Collaborator
University Hospital of Wales Danderyd Hospital, Hull and East Yorkshire Hospitals NHS Trust, Leuven University, Universitat Pompeu Fabra

Countries where clinical trial is conducted

Belgium,  Sweden,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnostic accuracy of quantitative measures of dobutamine stress echocardiography Echocardiographic measurements of segmental myocardial velocity, strain, strain rate and wall motion scoring referenced against measurements derived from coronary angiography. 18 months
Secondary Lowest dose of dobutamine to provoke measurable marker of inducible myocardial ischaemia Using modelling techniques applied predict lowest dose of dobutamine to maintain diagnostic accuracy 18 months
Secondary Diagnostic accuracy of using machine learning to interpret multiparametric and multidimensional datasets to diagnose myocardial ischaemia Use modelling to combine pre-test probabilities (based on risk factors such as age), physiological factors (e.g., heart rate) that are associated with longitudinal function and data derived throughout the cardiac cycle (i.e., based on analysis of velocity or strain curves and not just a single value like peak velocity or strain). 18 months
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