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Clinical Trial Summary

Patients with hypertrophic cardiomyopathy are being compared to a control group. IMR will be assessed with a pressure wire. Clinical f/u at 3 months and 6 months and a 48 hour holter monitor.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT02994615
Study type Observational
Source Lawson Health Research Institute
Status Completed
Start date January 2017
Completion date June 2020

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