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Clinical Trial Summary

This is a minimal risk case-controlled single arm intervention study, including 10 patients with a prior history of takotsubo and 10-age and sex matched healthy controls. Subjects will undergo in laboratory testing to measure autonomic function. They will then undergo a 15-week program of device-guided breathing with remote measures of autonomic function obtained at home. Analysis will determine the reproducibility of home autonomic measures and the provide preliminary data to determine the efficacy of device-guided breathing on autonomic measures and quality of life in patients with takotsubo.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03324529
Study type Interventional
Source NYU Langone Health
Contact Harmony Reynolds
Phone 646-501-0302
Email brokenheartstudy@nyumc.org
Status Recruiting
Phase N/A
Start date October 1, 2021
Completion date June 2025

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