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Registry of Patients With Takotsubo Syndrome

NYU Takotsubo (Broken Heart Syndrome) Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03663348
Enrollment
500
Registered
2018-09-10
Start date
2009-09-11
Completion date
2029-08-01
Last updated
2025-12-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Broken Heart Syndrome, Tako-tsubo Cardiomyopathy, Takotsubo Cardiomyopathy

Brief summary

Takotsubo syndrome is a condition which mimics acute myocardial infarction, and is diagnosed in 1.5% to 2.2% of patients referred to hospital with suspected acute coronary syndrome. It is also known as broken heart syndrome, takotsubo cardiomyopathy, stress cardiomyopathy and apical ballooning cardiomyopathy, among other names. The pathogenesis of this disorder is not well understood. Possible mechanisms include catecholamine excess, coronary artery spasm, microvascular dysfunction, among others. This is a multicenter, nation-wide, observational study of patients who were previously diagnosed with takotsubo syndrome. The investigators aim to use this registry to help plan and carry out further studies and to improve understanding of the pathophysiologic mechanisms of this syndrome. In addition participants will be followed for events, and to monitor quality of life and stress.

Detailed description

Patients are eligible to participate if they are aged 18 years or older and carry a physician confirmed diagnosis of takotsubo syndrome. Patients with a history of takotsubo syndrome will be identified via physician referral, Epic search and patient self-referral. Patients may register directly through our registry website at www.nyulmc.org/brokenheartstudy or via direct contact with the study team via e-mail or telephone. Following completion of a research authorization form and collection of medical records, study team will confirm the diagnosis of takotsubo syndrome. Data will be collected including contact information, medical history, data on the takotsubo event(s) including physician records and all relevant imaging. Participants will also be asked quality of life questionnaires and will be followed every 4 months for events.

Interventions

None listed

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 110 Years
Healthy volunteers
No

Inclusion criteria

* Physician diagnosis of takotsubo syndrome * Age\>18 years

Exclusion criteria

\- Lack of capacity to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Major Adverse Cardiac Eventsup to 10 yearsMedical record review and patient report of repeat takotsubo event, MI, heart failure, unstable angina, chest pain ER visit, cardiovascular death, stroke

Secondary

MeasureTime frameDescription
Quality of life assessed using the Patient Reported Outcome Measurement Information System (PROMIS-10) questionnaireevery four months up to 10 yearsMeasure of quality of life
Anxiety is assessed using the Hospital Anxiety and Depression Scale (HADS-A)every four months up to 10 yearsMeasure of anxiety
Depression assessed using the Patient Health Questionnaire (PHQ-9)every four months up to 10 yearsMeasure of depression
Perceived stress is measured using the Perceived Stress Scale (PSS-10)every four months up to 10 yearsMeasure of perceived stress

Countries

United States

Contacts

Primary ContactHarmony Reynolds, MD
brokenheartstudy@nyumc.org
Backup ContactAnais Hausvater, MD
brokenheartstudy@nyumc.org

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026