Heart Disease Trial, Recruiting NCT05492110 Sponsor: Imperial College London Condition: Heart Disease
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Heart Disease Trial, Recruiting

NCT05492110
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are over 18 years of age
  • People who have had ongoing chest pain (angina) symptoms rated as moderate to severe for at least 3 months, even while taking at least two anti-anginal (chest pain) medicines at the highest doses they can tolerate
  • People who are willing to keep their current chest pain medicines unchanged for the entire duration of the trial
  • People whose heart arteries do not have significant blockages (no more than 50% narrowing), as confirmed by a heart artery imaging test (coronary angiography)
  • People whose heart scan (a type of MRI called CMR) shows reduced blood flow to the heart muscle during stress testing, based on a specific measurement (confirm with trial site)
  • People who are willing to attend all required follow-up appointments and remain contactable throughout the trial
  • People who understand what the trial involves and have signed a written consent form

Who may not be able to join:

  • People who have significant blockages in a main heart artery (more than 50% narrowing, or abnormal pressure measurements), have had heart bypass surgery, or have had a heart attack
  • People who have had a heart artery procedure (PCI) within the past 6 months
  • People who have previously had a stent placed during a heart attack or to open a completely blocked artery
  • People with an unusual shape or structure of the coronary sinus (a vein near the heart) — including unusual bends, extra branches, or an abnormal vein on the left side of the chest
  • People whose coronary sinus is too narrow (under 9.5mm) or too wide (over 13mm) at the location where a device would be placed
  • People whose right atrium (a heart chamber) has a pressure measurement below a certain level at the time of the procedure (confirm with trial site)
  • People with certain structural heart conditions, including an enlarged heart muscle, heart muscle disease, severe heart valve disease, a previous heart valve replacement, a muscular band pressing on a heart artery, or reduced pumping function of the heart (less than 45% by heart MRI)
  • People who have been diagnosed with coronary vasospasm (sudden tightening of the heart arteries), either by symptoms or by imaging
  • People who have previously been hospitalised for severe heart failure
  • People who have a pacemaker or defibrillator lead (wire) located in the right side of the heart or the coronary sinus
  • People who have a documented irregular heart rhythm that means a permanent pacemaker or defibrillator is planned
  • People with significant kidney disease (based on blood test results, being on dialysis, or having a kidney transplant)
  • People with a low red blood cell level (haemoglobin below 80g/L)
  • People who cannot take a specific type of blood-thinning medicine combination (dual antiplatelet therapy)
  • People with severe chronic lung disease, based on breathing test results
  • People who are very unwell and are not expected to live longer than one year
  • People with a known allergy to nickel or steel
  • People who are currently taking part in another clinical trial of an investigational device or drug
  • People who cannot safely have a heart MRI scan or receive a specific medicine used during the scan (adenosine)
  • People who are pregnant

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 19 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Ranil E de Silva, FRCP, PhD, Imperial College London

Phone: +44 2073518626

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
17 April 2023
Est. completion
6 March 2026

Where this trial is recruiting

🇬🇧 United Kingdom

Primary endpoints

number of patients consenting to participate in the study.; Premature withdrawal rate including reasons for withdrawal; Change in myocardial perfusion

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov