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Coronary Sinus Reducer Objective Impact on Symptoms, MRI Ischaemia and Microvascular Resistance — ORBITA-COSMIC  

Refractory Angina Clinical Trial

Official title:
Coronary Sinus Reducer Objective Impact on Symptoms, MRI Ischaemia and Microvascular Resistance

Clinical Trial Summary

ORBITA-COSMIC is a randomised, double-blinded, placebo controlled trial of the coronary sinus reducer (CSR). The investigators will compare the effects of CSR versus placebo on myocardial perfusion on MRI, exercise time and symptoms in 50 participants with refractory angina and ischaemia.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04892537
Study type Interventional
Source Imperial College London
Contact Rasha Al-Lamee, PhD MRCP
Phone 020 7594 5735
Email r.al-lamee13@imperial.ac.uk
Status Recruiting
Phase N/A
Start date May 21, 2021
Completion date January 2024
View Details
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