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Coronary Sinus Reducer Objective Impact on SymptoMs, Ischaemia and miCrovascular Resistance in Non-obstructive Hypertrophic CardioMyopathy
Sponsor: Imperial College London
Summary
Hypertrophic cardiomyopathy (HCM) is a common heart condition in which the heart muscle becomes abnormally thick. In non-obstructive HCM, blood flow out of the heart is not blocked, but many patients still experience chest pain, breathlessness and limitation of daily activities. This may be because the small blood vessels within the thickened heart muscle do not supply enough blood and oxygen, particularly during exercise or stress. Current treatment options for symptomatic non-obstructive HCM are limited. This study will test a small device called the coronary sinus reducer (CSR), which is placed into a vein of the heart using a catheter. The CSR is designed to improve blood flow to areas of heart muscle that are short of blood supply. Fifty adults with non-obstructive HCM, ongoing symptoms and reduced blood supply on a heart MRI scan will take part. Participants will be randomly assigned to receive either CSR implantation or a placebo procedure. Neither participants nor the follow-up research team will know which procedure was performed until the 6-month follow-up assessments are complete. The investigators will use detailed heart MRI scans to measure blood flow, a smartphone app to record daily symptoms, coronary sinus blood tests to look for biochemical evidence of reduced oxygen supply, and invasive coronary physiology measurements to assess the small blood vessels of the heart. The main aim is to find out whether the CSR improves blood flow and reduces symptoms. The results may identify a new treatment option for patients with non-obstructive HCM and improve understanding of the disease.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
50
Start Date
2026-10-01
Completion Date
2029-09
Last Updated
2026-10-08
Healthy Volunteers
No
Conditions
Interventions
Coronary sinus reducer
The Shockwave Reducer (coronary sinus reducer) is intended to create a controlled narrowing that increases coronary sinus pressure and redistributes venous blood flow from epicardial to subendocardial regions, thereby improving myocardial perfusion in areas of microvascular ischaemia.
Placebo procedure
Participants in the placebo group will not have the device implanted, but will remain sedated in the catheter laboratory for 15-30 minutes so that the experience is similar and blinding is maintained.
Locations (8)
University Hospitals Bristol and Weston Nhs Foundation Trust
Bristol, United Kingdom
Liverpool Heart and Chest Hospital Nhs Foundation Trust
Liverpool, United Kingdom
Barts Health Nhs Trust
London, United Kingdom
Guy'S and St Thomas' Nhs Foundation Trust
London, United Kingdom
Imperial College Healthcare NHS Trust
London, United Kingdom
Oxford University Hospitals Nhs Foundation Trust
Oxford, United Kingdom
University Hospitals Dorset Nhs Foundation Trust
Poole, United Kingdom
Mid and South Essex Nhs Foundation Trust
Westcliff-on-Sea, United Kingdom