Coronary Flow During Rapid Heart Rates

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorImperial College London

About this trial

The goal of this observational study is to learn about the factors which determine how well ventricular tachycardia (VT) is tolerated. The main questions it aims to answer are:

1. What impact does coronary artery disease have on the ability for a patient to tolerate VT? 2. Does treatment of coronary artery disease with stents improve the tolerability of VT?

Participants who are undergoing a clinically indicated coronary angiogram or coronary angioplasty procedure will have measurements of blood pressure, coronary pressure and coronary flow made during pacing at a range of heart rates.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Able to give valid consent

Referred for coronary angiography or coronary angioplasty

Suitable for percutaneous physiological interrogation and PCI when clinically indicated

Disqualifiers

Unable to give valid consent

Pregnant or breastfeeding women

Unstable coronary artery disease (acute coronary syndrome)

Severe multivessel coronary artery disease suitable for coronary artery bypass grafting

Trial population

Adults referred for coronary angiography or coronary angioplasty.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Pressure and flow measurement during simulated VT

    Diagnostic test

    Participants undergoing coronary angiography will have measurements of blood pressure, coronary pressure and coronary flow during simulated VT. VT will be simulated using pacing at a range of heart rates.

Treatment groups

70 Participants
are divided into 4 treatment groups
Group A: Controls1 intervention
Group B: Coronary artery disease1 intervention
Group C: Microvascular dysfunction1 intervention
Group D: Heart failure1 intervention

Trial outcomes

Primary outcomes

1

Change in coronary flow in participants with different levels of coronary microvascular function.

Time frame
At baseline and during simulated VT
2

Change in coronary flow in participants immediately before and after PCI

Time frame
At baseline and during simulated VT, immediately before PCI and after PCI
3

Change in blood pressure in participants with different levels of coronary microvascular function.

Time frame
At baseline and during simulated VT
4

Change in blood pressure in participants before and after PCI

Time frame
At baseline and during simulated VT, immediately before PCI and after PCI

Secondary outcomes

1

Change in coronary flow in participants with different levels of left ventricular function

Time frame
At baseline and during simulated VT
2

Change in blood pressure in participants with different levels of left ventricular function

Time frame
At baseline and during simulated VT

Other outcomes

Sponsors and contacts

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